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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Molecular diagnosis of Prader-Willi syndrome (SNRPN and MAGEL2 genes; NGS)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (SNRPN gene)
    • CHU de Nantes - Institut de Biologie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Accreditation
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Laboratoire de biologie médicale GEN-BIO
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • AUVERGNE
    • CLERMONT-FERRAND
    • Accreditation
    • Molecular cytogenetic and molecular diagnosis of Prader-Willi syndrome (SNRPN, MAGEL2 genes and microsatellites, QMPSF techniques)
    • CHU de Toulouse - Hôpital Purpan
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi syndrome
    • Laboratoire Cerba
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • SAINT-OUEN-L'AUMÔNE
    • Accreditation
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Biomnis
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • RHONE-ALPES
    • LYON
    • Accreditation
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • LABOGEN S.a.S.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Accreditation
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (15q11-13)
    • University Hospitals Leuven - Gasthuisberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Postnatal molecular cytogenetics diagnosis of Prader-Willi/Angelman (uniparental disomy studies, methylation analysis and FISH of SNRP gene)
    • Azienda Ospedaliero Universitaria Careggi
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene: MS-MLPA, microsatellites)
    • Universitätsklinikum Essen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (UBE3A gene)
    • Labor Lademannbogen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Institut für Humangenetik am Universitätsklinikum Heidelberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Institut für Humangenetik am Universitätsklinikum Jena
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Thüringen
    • JENA
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Medizinisches Versorgungszentrum Humane Genetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome
    • Paxis und Labor Dr. med Karl Mehnert
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Institut für Medizinische Genetik und angewandte Genomik Tübingen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene: methylation analysis, MLPA)
    • Universitätsklinikum Ulm
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Medizinische Universität Innsbruck
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome. SNRPN gene
    • Laboratorio de Análisis Dr. Echevarne
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN, UBE3A genes)
    • Medizinische Hochschule Hannover
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (MS - MLPA)
    • Hôpitaux Universitaires de Genève HUG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular cytogenetics diagnosis (FISH) of Prader-Willi syndrome
    • Genetica AG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi syndrome (karyotyping; FISH; methylation sensitive MLPA; microarray; microsatellites for UPD15)
    • Universität Zürich
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Uniparental disomy study, Methylation analysis, Detection of chromosome alterations large in size
    • Technical procedure(s) : MLPA based techniques, Array based techniques, FISH, Karyotyping
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome
    • Center for Medical Genetics Ghent
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (PWCR)
    • CHU de LIEGE - UniLab Lg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Accreditation
    • Molecular cytogenetics diagnosis (FISH) of Prader - Willi syndrome
    • Centre Hospitalier Universitaire Vaudois CHUV
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by array-CGH
    • Centre Hospitalier Universitaire Vaudois CHUV
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome
    • University Hospital of Antwerp - UZA- Centrum Medische Genetica - CMG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular (methylation-sensitive MLPA) and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Heinrich-Heine-Universität Düsseldorf
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (15q11-q13 by methylation sensitive PCR)
    • St Mary's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (gene NDN or SNRPN)
    • Liverpool Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (by methylation specific PCR and Molecular diagnosis of Angelman syndrome (by methylation specific PCR and diagnosis by using markers outside the PWS region)
    • Southern General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • UNITED KINGDOM
    • Lanarkshire
    • GLASGOW
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Medizinische Universität Graz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Accreditation
    • Search for uniparental disomy (chromosomes 6, 7, 11, 14, 15 and/or 20)
    • Hôpitaux Universitaires de Genève HUG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (15q11-13)
    • Birmingham Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Mitteldeutscher Praxisverbund Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of uniparental disomy of chromosomes 2, 5-9, 11, 13-16, 18 and 22
    • Mitteldeutscher Praxisverbund Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome through methylation sensitive MLPA analysis (NDN, SNRPN genes)
    • Nottingham City Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Nottinghamshire
    • NOTTINGHAM
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays / chromosomal microarrays
    • Universität Zürich
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (Methylation-specific MLPA of the SNPRN gene,15q11-q13, UPD and deletion analysis)
    • Salisbury District Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Wiltshire
    • SALISBURY
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Centrum für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Hessen
    • BAD NAUHEIM
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Zentrum für Humangenetik Mannheim
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular cytogenetics diagnosis of Prader-Willi
    • Biomnis
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Medizinische Versorgungszentrum Dr.Stein + Kollegen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÖNCHENGLADBACH
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (by conventional karyotype and FISH analysis)
    • St Mary's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : FISH, Karyotyping
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of uniparental disomy (chromosome 7, 14, 15)
    • Erasme Hospital - ULB
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (methylation SNRPN gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (SNRPN gene: Targetted mutation analysis / gene tracking)
    • St George's University of London
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Prader - Willi Syndrome
    • Centre Hospitalier Universitaire Vaudois CHUV
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Uniparental Disomy (any chromosome)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular Diagnosis of Prader-Willi Syndrome (critical region)
    • National Centre for Medical Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • IRELAND
    • County Dublin
    • DUBLIN
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (methylation SNRPN gene)
    • Erasmus MC, Faculteitsgebouw
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of Prader Willi syndrome (SNRPN gene)
    • Addenbrooke's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of Prader-Willi Syndrome (SNRPN methylation)
    • AMC - Academisch Medisch Centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Prader-Willi Syndrome (methylation 15q11-q13)
    • Radboudumc - Radboud universitair medisch centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Institut für Klinische Genetik Mainz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Schleswig-Holstein
    • LÜBECK
    • Accreditation
    • Molecular diagnosis of uniparental disomyof chromosomes 14, 15 and 16
    • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • GERMANY
    • Schleswig-Holstein
    • LÜBECK
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene: targeted mutation analysis / gene tracking)
    • International Centre for Life
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (MS-MLPA of region 15q11-13)
    • The Churchill Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of uniparental disomy of chromosomes 7, 14 , 15 and X
    • Institut für Humangenetik am Universitätsklinikum Heidelberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome
    • Erasme Hospital - ULB
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of uniparental disomy of chromosomes 6, 7, 11, 14, 15
    • Medizinisches Versorgungszentrum Humane Genetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (methylation status/MLPA of region 15q11.2, msMLPA of region 15q11-13)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of Prader-Willi Syndrome (Methylation analysis and UPD15)
    • AZM - Academisch Ziekenhuis Maastricht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Accreditation
    • Molecular diagnosis of Uniparental Disomy (UPD7, UPD14, UPD15 and UPD16)
    • AZM - Academisch Ziekenhuis Maastricht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Angelman / Prader-Willi syndrome (FISH at the D15S10 locus; SNRPN gene: Southern blot)
    • Lund University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SWEDEN
    • Skane
    • LUND
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (by conventional karyotype and FISH analysis)
    • Our Lady's Children's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : FISH, Karyotyping
    • More information
    • IRELAND
    • County Dublin
    • DUBLIN
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome/Angelman syndrome (methylation status of SNRPN promoter, MLPA)
    • Universitätsmedizin Mainz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • Molecular diagnosis of uniparental disomy (6, 7, 14, 15) by microsatellite analysis
    • Universitätsmedizin Mainz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • MLPA analysis of microdeletion syndrome regions
    • Universitätsmedizin Mainz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (by FISH analysis)
    • Liverpool Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH at 15q11-q13 locus)
    • Yhtyneet Medix Laboratoriot
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome by FISH
    • FIMLab Laboratories
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FINLAND
    • Finland
    • TAMPERE
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • MVZ Labor Dr. Reising-Ackermann und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Sachsen
    • LEIPZIG
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (methylation analysis by RFLP)
    • BioAnalytica-GenoType SA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Accreditation
    • Diagnosis of microdeletion and microduplication syndromes by FISH and array CGH
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : Array based techniques, FISH
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (by FISH analysis)
    • Birmingham Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Prader-Willi Syndrome (15q11-q13)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Prader Willi Syndrome
    • Université Catholique de Louvain - UCL
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (MS-MLPA of region 15q11-13)
    • Medizinisches Versorgungszentrum Humane Genetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis)
    • Sahlgrenska university hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SWEDEN
    • Västra Götalandsregionen
    • GÖTEBORG
    • Accreditation
    • Molecular diagnosis of Prader-Willi and Angelman syndromes (methylation defects at SNRPN locus and UBE3A gene mutations)
    • CHU de Marseille - Hôpital de la Timone
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (by FISH and MLPA testing at 15q11-13)
    • St James's University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis at locus 15q11-q13)
    • Southmead Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis at locus 15q11-q13)
    • Norfolk and Norwich University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Norfolk
    • NORWICH
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis)
    • St George's University of London
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene: by MLPA and methylation studies)
    • The Doctors Laboratory Ltd
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene: methylation status, STR analysis)
    • GenteQ GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (methylation-MLPA, UBE3A gene: sequencing)
    • Diagenom GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome/Angelman syndrome (methylation status)
    • MVZ Fenner & Krasemann
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (methylation status)
    • Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome due to deletion, translocation, or uniparental disomy
    • Biomnis
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Deletion / Duplication analysis
    • More information
    • FRANCE
    • RHONE-ALPES
    • LYON
    • Accreditation
    • Molecular Diagnosis of Prader-Willi syndrome (by methylation and copy number MLPA and UPD analysis)
    • The Hospital for Sick Children and University of Toronto
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molecular cytogentic diagnosis (FISH) of Prader-Willi syndrome
    • Aurigen - Centre Romand de génétique et de pathologie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Labor PD Dr. Volkmann und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Cytogenetic diagnosis of Prader-Willi syndrome (FISH of SNRPN gene)
    • CHU de Nice - Hôpital l'Archet 2
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Molecular diagnosis of Prader-Willi-like syndrome (MAGEL2 gene)
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Prader-Willi Syndrome (UPD15 studies: SNRPN gene: targetted mutation analysis)
    • Birmingham Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Male Infertility Due To Y Chromosome Deletions (DDX3Y, DAZ1, DAZ2, DAZ3, USP9Y genes: Targetted mutation analysis / Testing for known mutations in family members)
    • St George's University of London
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular Diagnosis of Male Infertility Due To Y Chromosome Deletions (DDX3Y, DAZ1, DAZ2, DAZ3, USP9Y genes: targeted mutation analysis)
    • Salisbury District Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis
    • More information
    • UNITED KINGDOM
    • Wiltshire
    • SALISBURY
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome
    • Synlab Lausanne
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular Diagnosis of Prader-Willi syndrome (MLPA)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Manitoba
    • WINNIPEG
    • Accreditation
    • Molecular Diagnosis of Prader Willi Syndrome (MS-MLPA)
    • Children's Hospital of Eastern Ontario
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Ontario
    • OTTAWA
    • Accreditation
    • Molecular Diagnosis of Prader Willi Syndrome (MS-MLPA)
    • North York General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molecular Diagnosis of UPD 15 (microsatellite analysis)
    • North York General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molekulare Diagnostik des Prader-Willi-Syndroms
    • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Institut für angewandte Humangenetik und Onkogenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Accreditation
    • Molecular diagnosis of Prader-Willi syndrome by targetted copy number analysis (NDN gene)
    • Belfast City Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Antrim and Newtownabbey
    • BELFAST
    • Accreditation
    • Molecular cytogenetic diagnosis of Prader-Willi and Angelman syndromes (FISH analysis at locus 15q11-q13)
    • CYTOGEN
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • SAINT-HERBLAIN
    • Accreditation
    • Molecular Diagnosis of Male Infertility Due To Y Chromosome Deletions (DDX3Y, DAZ1, DAZ2, DAZ3, USP9Y genes: targeted mutation analysis / Testing for known mutations in family members)
    • St James's University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Accreditation
    • Molecular Cytogenetic Diagnosis of Prader Willi/Angelman Syndrome (mFISH SNRPN probe analysis)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • CANADA
    • Terre-Neuve-et-Labrador
    • ST. JOHN'S
    • Accreditation
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi syndrome (MS-MLPA)
    • CHU de Nancy - Hôpital de Brabois
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LÈS-NANCY
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • CHU de Strasbourg - Hôpital Civil
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ALSACE
    • STRASBOURG
    • Molecular diagnosis of Prader-Willi syndrome (methylation, microsatellite)
    • CHU Paris Centre - Hôpital Cochin
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU de Marseille - Hôpital de la Timone
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • CHRU de Lille - Hôpital Jeanne de Flandre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU de Lyon HCL - GH Est
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi syndrome by methylation studies of 15q11-q13 region by specific M-PCR
    • CHU de Saint-Etienne - Hôpital Nord
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • RHONE-ALPES
    • SAINT-PRIEST-EN-JAREZ
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU de Dijon - Plateau technique de Biologie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • BOURGOGNE
    • DIJON
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU Paris - Hôpital Robert Debré
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU Paris Centre - Maternité Port Royal
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of Angelman and Prader-Willy syndromes (15q11q13 deletion)
    • CHU de Poitiers
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • POITOU-CHARENTES
    • POITIERS
    • Molecular diagnosis of Prader-Williand Angelman syndromes (MLPA: 15q11q13 region, methylation analysis of SNRPN gene)
    • CHU de Poitiers
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • FRANCE
    • POITOU-CHARENTES
    • POITIERS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Laboratoire BIOFFICE
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (methylation study of SNRPN locus by PCR)
    • CHU de Reims - Hôpital Maison Blanche
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Preimplantation and postnatal cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis of SNRPN gene)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Purpose(s) : Pre-implantation diagnosis, Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU de Rouen - Hôpital Charles Nicolle
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Molecular and cytogenetic diagnosis of Prader Willi syndrome (SNRPN gene)
    • CH de Versailles - Hôpital André Mignot
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • LE CHESNAY
    • Molecular diagnosis of Prader Willi syndrome by RT-PCR and methyl-sensitive MLPA (SNRPN gene)
    • CHU Paris - Hôpital Robert Debré
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : PCR based techniques, MLPA based techniques
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHRU de Besançon - Hôpital Saint-Jacques
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • FRANCHE-COMTE
    • BESANÇON
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Laboratoire de Biologie Clinique
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • LORRAINE
    • NANCY
    • Molecular diagnosis of Prader-Willi syndrome
    • Faculté de médecine et de pharmacie de Rouen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Molecular cytogenetics prenatal and postnatal diagnosis of Prader-Willi syndrome
    • CHU de Nantes - Institut de Biologie
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • CHU de Bordeaux-GH Pellegrin
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular cytogenetics diagnosis of Prader Willi/Angelman syndrome
    • Ospedali Galliera
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • BIOS S.p.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome (UBE3A gene)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of Prader-Willi/Angelman syndrome (SNRPN, UBE3A genes)
    • Istituto Auxologico Italiano
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • CUSANO MILANINO
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Istituti Ospitalieri di Cremona
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • CREMONA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS Istituto Auxologico Italiano - Ospedale San Michele
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • ASLRMA - Centro per la tutela della Salute della Donna e del Bambino
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN, SNORD116@ genes)
    • Corporación Sanitaria Parc Taulí
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • SABADELL
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Santa Maria degli Angeli
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • PORDENONE
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Laboratorio Genoma
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Praenatal-Medizin und Genetik, Düsseldorf
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Molecular diagnosis of Prader-Willi syndrome (methylation status of SNRPN promoter)
    • Humangenetisches Institut am Universitätsklinikum Erlangen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Bayern
    • ERLANGEN
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera- Ospedale Civile di Legnano
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • LEGNANO
    • Postanatal molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome (FISH analysis)
    • Università degli Studi di Milano - Biologia e Genetica per le Scienze Mediche
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • SIENA
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Ospedali Riuniti "Umberto I - G.M. Lancisi - G. Salesi" - Presidio "G. Salesi"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • MARCHE
    • ANCONA
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Ospedale Regionale per le Microcitemie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Search for uniparental disomy
    • Centro de Análisis Genéticos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman
    • Laboratorio Analisi CITOTEST
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • SARMEOLA DI RUBANO
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS Ospedale San Raffaele
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Ospedali Riuniti di Bergamo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • BERGAMO
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Università degli Studi di Pavia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • PAVIA
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome (SNRPN gene)
    • CHU de Nîmes - Hôpital Caremeau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • NÎMES
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Centro de Análisis Genéticos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelamn syndrome
    • Ospedale Civile S.S. Giovanni e Paolo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • VENEZIA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Ospedale "San Bassiano"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • BASSANO DEL GRAPPA
    • Cytogenetic diagnosis of Prader-Willi/Angelman
    • AUSL Cesena
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • PIEVESESTINA DI CESENA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera "San Paolo" - Università degli Studi di Milano
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • ULSS 6 "Vicenza"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • VICENZA
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi/Angelman syndromes
    • A.O.U. di Ferrara - Polo Chimico-Bio-Medico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • FERRARA
    • Molecular diagnosis of uniparental disomy of chromosomes 7, 14 and 15 (SNRPN and UBE3A genes)
    • CH de Versailles - Hôpital André Mignot
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • LE CHESNAY
    • Molecular diagnosis of Prader-Willi syndrome (deletions or changes in the methylation pattern of 15q11-q13 region; detection of uniparental disomy)
    • Hospital Universitario Virgen del Rocío
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis, Deletion / Duplication analysis
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome (FISH, Caryotype, MS-MLPA: 15q11q13 region BP1 to BP3, microsatellites)
    • CHU de Limoges - Hôpital de la mère et de l'enfant
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • FRANCE
    • LIMOUSIN
    • LIMOGES
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Landes- Frauen- und Kinderklinik Linz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • AUSTRIA
    • OBERÖSTERREICH
    • LINZ
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome with methylation analysis, FISH, UPD
    • Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of Prader-Willi syndrome
    • Universitätsspital Basel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BASEL
    • Molecular diagnosis of uniparental disomy of chromosomes 7, 14 and 15 by studying microsatellites (study of Copy Number Variation)
    • CHU de Caen - Hôpital Clémenceau
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU d'Amiens - Hôpital Sud
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • PICARDIE
    • AMIENS
    • Molecular diagnosis of Prader-Willi syndrome
    • Turku University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular cytogenetics and molecular diagnosis of Prader Willi syndrome
    • Oulu University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • FINLAND
    • Finland
    • OULU
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Institut für Humangenetik der Martin-Luther-Universität Halle Wittenberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Sachsen-Anhalt
    • HALLE (SAALE)
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • University Hospitals Leuven - Gasthuisberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Universitätsklinikum Bonn
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular cytogenetics diagnosis of Angelman and Prader-Willi syndromes (15q11-q13): FISH/MLPA
    • Faculdade de Medicina da Universidade do Porto
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Faculdade de Medicina da Universidade do Porto
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular and cytogenetic diagnosis of Prader Willi syndrome (methylation, microdeletion and FISH)
    • Kennedy Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis, Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • DENMARK
    • Sjælland
    • GLOSTRUP
    • Molecular diagnosis of Prader-Willi syndrome
    • LKH Salzburg - Universitätsklinikum der Paracelsus Med. Privatuniversität
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • SALZBURG
    • SALZBURG
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Praxis Dres. Gencik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Medizinische Universität Wien
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Klinikum Stuttgart - Standort Olgahospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Complejo Hospitalario de Navarra - Hospital Virgen del Camino
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • SPAIN
    • Navarra
    • PAMPLONA
    • Molecular diagnosis of Prader-Willi syndrome
    • Rigshospitalet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • DENMARK
    • Hovedstaden
    • COPENHAGEN
    • Molecular diagnosis of uniparental disomy
    • Rigshospitalet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • DENMARK
    • Hovedstaden
    • COPENHAGEN
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi syndrome (SNRPN gene / MLPA, microsatellites and FISH)
    • Hospital Universitario Miguel Servet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of Prader-Willi syndrome (15q11-q13)
    • Praxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi syndrome (MAGEL2, NDN, SNRPN, OCA2 genes)
    • Fundación Jiménez Díaz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Prader Willi syndrome
    • Aarhus Universitetshospital - Skejby
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • DENMARK
    • Jylland
    • AARHUS
    • Molecular diagnosis of Prader-Willi syndrome (a-CGH, MLPA and FISH)
    • Leto Maternity Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques, Array based techniques, FISH
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Diagnostic Genetic Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of Prader-Willi syndrome screening for methylation of SNRPN gene
    • Tartu University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Laboratoire d'analyses médicales Clément
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • LE BLANC MESNIL
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Toma Advanced Biomedical Assays S.p.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • BUSTO ARSIZIO
    • Molecular diagnosis of Prader-Willi syndrome (detection of microdeletion or uniparental disomy 15q11-13)
    • Hospital Universitario Central de Asturias
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • SPAIN
    • Asturias
    • OVIEDO
    • Molecular diagnosis of Prader-Willi syndrome
    • Centro de Bioquímica y Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Murcia
    • EL PALMAR
    • Molecular (MLPA, UPD, UBE3A sequencing) and molecular cytogenetic (FISH) diagnosis of Prader-Willi/Angelman syndrome (15q11-13 region ;UBE3A gene)
    • B.I.R.D. Foundation
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of Prader-Willi syndrome
    • Oslo University Hospital, Ullevaal
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NORWAY
    • Østlandet
    • OSLO
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Haukeland University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • NORWAY
    • Vestlandet
    • BERGEN
    • Molecular genetics diagnosis of Prader-Willi syndrome
    • Uppsala University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWEDEN
    • Landstinget i Uppsala län
    • UPPSALA
    • Molecular diagnosis of Prader-Willi syndrome (methylation analysis at the SNRPN locus)
    • Instytut Matki i Dziecka
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • POLAND
    • Warszawa
    • WARSZAWA
    • Molecular diagnosis of Prader-Willi/Angelman syndrome (UB3A gene)
    • Azienda Ospedaliera di Padova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of Prader-Willi syndrome (MLPA)
    • Centro Inmunológico de Alicante (CIALAB)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHI Toulon La Seyne-sur-Mer - Hôpital Sainte Musse
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • TOULON
    • Cytogenetic and molecular diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Universitaria Anna Meyer
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome (SNRPN gene)
    • Istituto CSS-Mendel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Cytogenetic diagnosis of Prader-Willi syndrome (by conventional karyotype and FISH analysis)
    • Cambridge University Hospitals NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : FISH, Karyotyping
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Faculté de médecine de Clermont-Ferrand
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • AUVERGNE
    • CLERMONT-FERRAND
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Institut für Humangenetik des Universitätsklinikums Münster
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of Prader Willi syndrome (PWCR gene)
    • Karolinska University Hospital - Clinical Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of uniparental disomy
    • Karolinska University Hospital - Clinical Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Cytogenetic diagnosis of Prader-Willi syndrome (by FISH analysis)
    • University Medical Center Ljubljana
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SLOVENIA
    • SLOVENIA
    • LJUBLJANA
    • Molecular diagnosis of Prader-Willi syndrome (methylation status)
    • Institut für Klinische Genetik Bonn
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of Prader-Willi and Angelman syndromes (SNRPN gene)
    • CHRU de Besançon - Hôpital Saint-Jacques
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • FRANCHE-COMTE
    • BESANÇON
    • Molecular diagnosis of Prader-Willi / Angelman syndrome (microdeletion and methylation defects at locus 15q11-q13 detected by MLPA)
    • Sygehus Lillebaelt Vejle Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • DENMARK
    • Syddanmark
    • VEJLE
    • Molecular diagnosis of chromosomes 7, 14, 15 and 16 uniparental disomies
    • Sygehus Lillebaelt Vejle Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • DENMARK
    • Syddanmark
    • VEJLE
    • Cytogenetic diagnosis of Prader-Willi syndrome (by FISH analysis)
    • Ninewells Hospital and Medical School
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (by FISH at 15q11.2)
    • Guy's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Molecular diagnosis of Prader-Willi syndrome
    • Clinical Center - University of Pécs
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • HUNGARY
    • Dél-Dunántúl
    • PECS
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene: sequencing, MLPA)
    • bio.logis Zentrum für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome/Angelman syndrome (FISH/ microsatellites)
    • Pränatalzentrum Hamburg und Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular cytogenetic diagnosis of Prader-Willi and Angelman syndromes (FISH at 15q11-13)
    • Institute of Child Health
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular cytogenetic diagnosis of Prader-Willi and Angelman syndromes (by FISH)
    • Medical Genetics Laboratory
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • CZECH REPUBLIC
    • Hradec Kralove
    • HRADEC KRALOVE
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome by FISH
    • Bioiatriki S.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of Prader-Willi syndrome by MLPA
    • Mitera General, Maternity and Children's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of Prader-Willi syndrome
    • Przychodnia Fundacji Uniwersytetu Medycznego we Wroclawiu
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • POLAND
    • Wroclaw
    • WROCLAW
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome by methylation analysis and FISH analysis
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : FISH
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN locus methylation assay; uniparental disomy analysis)
    • CHU de Dijon - Plateau technique de Biologie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis
    • More information
    • FRANCE
    • BOURGOGNE
    • DIJON
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene; DNA methylation test)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • FISH analyses of microdeletions / microduplications
    • Centre hospitalier
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • LE MANS
    • Molecular cytogenetic analysis of microdeletions/microduplications (by FISH)
    • CHU de Grenoble site Nord - Hôpital Couple-Enfant
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis)
    • CHRU de Brest - Hôpital Morvan
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular cytogenetic diagnosis of Prader-Willi / Angelman syndrome (by FISH)
    • Intergen Genetics Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • TURKEY
    • TURKEY
    • ANKARA
    • FISH analysis of microdeletions / microduplications
    • CH de Mulhouse - Hôpital Emile Muller
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • ALSACE
    • MULHOUSE
    • Molecular cytogenetic diagnosis of Prader-Willi and Angelman syndromes (FISH analysis)
    • Mother and Child Care Institute IOMC "Prof. dr. Alfred Rusescu"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ROMANIA
    • BUCURESTI
    • BUCURESTI
    • Molecular diagnosis of Prader-Willi syndrome (methylation analysis and search for deletion in 15q11-q13)
    • MEDGEN
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis, Deletion / Duplication analysis
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • FISH analysis of the 15q11.3 microdeletion
    • CHU de Caen - Hôpital de la Côte de Nacre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis)
    • Western General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH analysis at locus 15q11-q13)
    • Belfast City Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Antrim and Newtownabbey
    • BELFAST
    • Cytogenetic diagnosis of constitutional chromosomal abnormalities (microdeletion/ microduplication syndromes by FISH, MLPA, array CGH: MLPA kits P245, P297, P036)
    • Instytut Matki i Dziecka
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
    • Technical procedure(s) : MLPA based techniques, Array based techniques, FISH, Karyotyping
    • More information
    • POLAND
    • Warszawa
    • WARSZAWA
    • Cytogenetic diagnosis of Prader-Willi syndrome (microdeletion 15q11-q13 by FISH analysis)
    • Uniwersyteckie Centrum Kliniczne
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • POLAND
    • Gdansk
    • GDANSK
    • Molecular diagnosis of Prader-Willi/Angelman syndromes
    • A.O.U. di Ferrara - Polo Chimico-Bio-Medico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • FERRARA
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Institut für Humangenetik am Universitätsklinikum Freiburg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular cytogenetics of Prader-Willi syndrome (by FISH analysis at locus 15q11-q13)
    • Hospital Universitario Donostia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of Prader-Willi syndrome (microsatellite analysis)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Prader-Willi syndrome (aCGH)
    • Genetadi Biotech S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of Prader-Willi and Angelman syndromes
    • INGEMM - Instituto de Genética Médica y Molecular
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Antenatal molecular diagnosis of chromosome 6, 7, 14, 15 uniparental disomy
    • ASLRMA - Centro per la tutela della Salute della Donna e del Bambino
    • Purpose(s) : Antenatal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of dysmorphological syndromes by CGH array
    • CHRU de Brest - Hôpital Morvan
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndromes
    • Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • UDINE
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi syndrome by MLPA and FISH
    • Faculdade de Medicina da Universidade de Coimbra
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular diagnosis of microdeletion syndromes (by MLPA kit P297 & P245)
    • Faculdade de Medicina da Universidade de Coimbra
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular diagnosis of microdeletion syndromes by MLPA (kit P245)
    • Hospital Universitario Son Espases
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Baleares
    • PALMA DE MALLORCA
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi syndrome due to paternal 15q11q13 deletion: diagnosis and prenatal testing (locus 15q11-q13 / FISH, MLPA, STR)
    • Hospital Clínico San Carlos
    • Purpose(s) : Antenatal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene)
    • Medizinische Universität Wien
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome due to paternal 15q11q13 deletion (15q11-q13 / FISH)
    • Hospital Universitario Príncipe de Asturias
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Madrid
    • ALCALÁ DE HENARES
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome/Angelman syndrome
    • Institut für Humangenetik Wiesbaden
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Hessen
    • WIESBADEN
    • Molecular diagnosis of Prader-Willi syndrome (methylation status of SNRPN promoter)
    • Laborärztlich-humangenetische Partnerschaft Eiben - Glaubitz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • Cytogenetic diagnosis of Prader-Willi and Angelman syndromes
    • CHR de Metz-Thionville
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • LORRAINE
    • METZ
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi syndrome due to paternal 15q11q13 deletion (FISH; array-CGH)
    • Policlínica Gipuzkoa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques, FISH
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of microdeletions syndromes (MLPA kit P245)
    • Policlínica Gipuzkoa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of mental retardation syndromes (MLPA kit P064)
    • Policlínica Gipuzkoa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene / MLPA)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of intellectual deficit due to microdeletions microduplications (SALSA MLPA kit P064)
    • Kennedy Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • DENMARK
    • Sjælland
    • GLOSTRUP
    • Molecular diagnosis of chromosomal anomalies (array-CGH)
    • NIMGenetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Cytogenetic diagnosis of Angelman and Prader-Willi syndromes (FISH)
    • CHU de Strasbourg - Hôpital de Hautepierre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • ALSACE
    • STRASBOURG
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi syndrome (array CGH, FISH, MLPA methylation)
    • Hospital Universitari General Vall d'Hebron
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques, Array based techniques, FISH
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene / MS-MLPA)
    • GenoClinics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Prenatal and postnatal molecular genetic and cytogenetics diagnosis of Prader-Willi syndrome (deletion/duplication analysis by MLPA, FISH and DNA methylation analysis)
    • Laboratório de Análises Clínicas Dr. Joaquim Chaves
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques, FISH
    • More information
    • PORTUGAL
    • CENTRO
    • OEIRAS
    • Molecular cytogenetics diagnosis of Prader Willi syndrome (Chromosome 15, 15q11-13 region: deletion analysis by FISH)
    • Universidade da Madeira
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • PORTUGAL
    • ILHAS
    • FUNCHAL
    • Molecular diagnosis of Prader-Willi / Angelman syndrome (methylation profile by MC-PCR + MS-MLPA)
    • Montreal Children's hospital - Hôpital de Montréal pour enfants
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis
    • Technical procedure(s) : PCR based techniques, MLPA based techniques
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome due to paternal 15q11q13 deletion (FISH)
    • Genetic Diagnóstico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • País Vasco
    • BILBAO
    • Preimplantation and postnatal molecular diagnosis of chromosomal anomalies (array-CGH)
    • Hospital Clínica Vistahermosa
    • Purpose(s) : Pre-implantation diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ALICANTE
    • Molecular cytogenetics diagnosis of Prader Willi/Angelman syndrome
    • Laboratori Campisi s.r.l.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • SICILIA
    • AVOLA
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome (FISH analysis)
    • CHU de la Réunion - Hôpital Félix Guyon
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • OUTRE-MER
    • SAINT-DENIS
    • Molecular Diagnosis Prader-Willi syndrome (MLPA/UPD-15 PWSCR)
    • Alberta Children's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Alberta
    • CALGARY
    • Molecular diagnosis of Prader-Willi-like syndrome (MAGEL2 gene)
    • Praxis Dres. Gencik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular Diagnosis of Prader-Willi Syndrome (D-PCR of SNRPN)
    • BC Women's Hospital and Health Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : PCR based techniques
    • More information
    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • Molecular Diagnosis Prader-Willi syndrome (MLPA/UPD-15 PWSCR)
    • University of Alberta
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Alberta
    • EDMONTON
    • Molecular Cytogenetic Diagnosis of Prader Willi/Angelman Syndrome (mFISH SNRPN probe analysis)
    • Alberta Children's Hospital
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • CANADA
    • Alberta
    • CALGARY
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome (determined by Prenatal BoBs)
    • TEST s.r.l.
    • Purpose(s) : Antenatal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • MODENA
    • Molecular diagnosis of Prader-Willi syndrome/Angelman syndrome
    • Praxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bremen
    • BREMEN
    • Molecular diagnosis of Prader-Willi syndrome/Angelman syndrome (methylation status)
    • MVZ wagnerstibbe für Laboratoriumsmedizin und Pathologie GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH)
    • Przychodnia Fundacji Uniwersytetu Medycznego we Wroclawiu
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • POLAND
    • Wroclaw
    • WROCLAW
    • Molecular diagnosis of Prader-Willi syndrome/Angelman syndrome (methylation status)
    • Praxis für medizinische Genetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • GH de l'Institut Catholique de Lille - Hopital Saint Vincent de Paul
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Clinique St Jean Languedoc
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU de Caen - Hôpital Clémenceau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU de Rennes - Hôpital Pontchaillou
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • BRETAGNE
    • RENNES
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome (FISH analysis)
    • CHU Paris Seine-Saint-Denis - Hôpital Jean Verdier
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • BONDY
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Hotel-Dieu
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • RHONE-ALPES
    • CHAMBERY
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHR d'Orléans - Hôpital de la Source
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • CENTRE
    • ORLEANS
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera San Gerardo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • MONZA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Policlinico Universitario di Chieti
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • ABRUZZO
    • CHIETI
    • Cytogenetic diagnosis of Prader-Will/Angelman syndrome
    • Ospedale di Venere - ASL Bari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • ITALY
    • PUGLIA
    • CARBONARA DI BARI
    • Molecular diagnosis of Prader-Willi/Angelman syndrome (SNRPN gene)
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular cytogenetics diagnosis of Prader Willi/Angelman syndrome
    • Ospedale San Martino
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • BELLUNO
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular cytogenetics diagnosis fo Prader-Willi/Angelman syndrome
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome (SNRPN and UBE3A genes)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Laboratorio Genoma
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Ospedale Santa Maria delle Croci
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • RAVENNA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman
    • Azienda Ospedaliera Universitaria "Federico II"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular cytogenetics diagnosis of Prader-Willi/Angleman
    • Università degli Studi di Sassari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • SARDEGNA
    • SASSARI
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Policlinico Universitario "A. Gemelli"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome (SNRPN gene)
    • Azienda Ospedaliera Universitaria Integrata di Verona - Ospedale Borgo Roma
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • VERONA
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • VARESE
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera San Giovanni Addolorata
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera BMM
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CALABRIA
    • REGGIO CALABRIA
    • Molecular cytogenetic and molecular diagnosis of Prader-Willi syndrome. Methylation analysis. FISH.
    • Complejo Hospitalario Universitario Insular-Materno Infantil
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Canarias
    • LAS PALMAS DE GRAN CANARIA
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome by FISH analysis at 15q11-13
    • Hospital Universitario de Móstoles
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Madrid
    • MÓSTOLES
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Pugliese Ciaccio
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • CALABRIA
    • CATANZARO
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Università degli Studi di Brescia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • BRESCIA
    • Molecular cytogenetics diagnosis of Parder-Willi/Angelman syndrome
    • Azienda Ospedaliera di Padova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Presidio Ospedaliero "Città di Sesto San Giovanni"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • SESTO SAN GIOVANNI
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • Ospedale Santa Chiara
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • TRENTINO ALTO ADIGE
    • TRENTO
    • Cytogenetic diagnosis of Prader-Willi/Angelman syndrome by high resolution
    • Poliambulatorio
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • UMBRIA
    • PERUGIA
    • Molecular cytogenetics diagnosis of chromosome anomalies
    • Hospital Perpetuo Socorro
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • SPAIN
    • Extremadura
    • BADAJOZ
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome by FISH analysis at 15q11-13
    • Hospital Universitario de Canarias
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Canarias
    • SANTA CRUZ DE TENERIFE
    • Molecular cytogenetics and molecular diagnosis of Prader-Willi syndrome (FISH, methylation analysis)
    • Complejo Hospitalario Universitario A Coruña
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Galicia
    • A CORUÑA
    • Cytogenetics molecular diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS OASI Maria Santissima
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • SICILIA
    • TROINA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • P.S.I. "Elena d'Aosta"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Università degli Studi dell'Aquila - Coppito
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • ABRUZZO
    • L'AQUILA
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Centro Hospitalar de Vila Real-Peso da Régua, SA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • PORTUGAL
    • NORTE
    • VILA REAL
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Ospedali Riuniti "Villa Sofia-Cervello" - Presidio Cervello
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • PALERMO
    • Molecular cytogenetic diagnosis of Padre-Willi/Angelman syndrome
    • Azienda Ospedaliera S. Anna
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • SAN FERMO DELLA BATTAGLIA
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Laboratoire BIOXA Porte de Paris
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Molecular and cytogenetic diagnosis of Prader-Willi syndrome
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of Prader-Willi/Angelmann
    • Centro Medico Artemisia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetics diagnosis of Prader-Willi/Angelman syndrome
    • AUSL di Imola
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • IMOLA
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular cytogenetics diagnosis (FISH) of Prader Willi syndrome
    • University Children's Hospital - UKBB
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BASEL
    • Molecular diagnosis of Prader-Willi syndrome
    • Medical school - University of Ioannina
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GREECE
    • IOANNINA
    • IOANNINA
    • Molecular diagnosis of Prader-Willi syndrome
    • "Aghia Sophia" Children's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Cytogenetics pre-natal and post-natal diagnosis of Angelman/Prader-Willi syndromes (by FISH)
    • CHRU de Montpellier - Hôpital Arnaud de Villeneuve
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS Burlo Garofolo - Istituto per l'Infanzia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • TRIESTE
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Associazione Cante di Montevecchio
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • MARCHE
    • FANO
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS "E. Medea"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • BOSISIO PARINI
    • Molecular Diagnosis of Prader-Willi Syndrome
    • Hospital Universitario Virgen de las Nieves
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • GRANADA
    • Molecular citogenetics diagnosis of Prader Willi/Angelman syndrome
    • Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • UDINE
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • IRCCS OASI Maria Santissima
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • TROINA
    • Molecular diagnosis of Prader Willi/Angelman syndrome
    • IRCCS Arcispedale Santa Maria Nuova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • REGGIO EMILIA
    • Molecular Cytogenetic Diagnosis of Prader-Willi Syndrome
    • Centro de Investigación sobre Anomalías Congénitas
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Prader-Willi syndrome : search for duplication and uniparental disomy (UPD) study
    • Motol university hospital - 2nd Medical School Charles University Prague
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Deletion / Duplication analysis
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular and molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Acibadem healthcare group
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of Prader-Willi/Angelman syndrome
    • Policlinico Universitario di Chieti
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • ABRUZZO
    • CHIETI
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera Universitaria di Perugia Santa Maria della Misericordia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • UMBRIA
    • PERUGIA
    • Molecular cytogenetic diagnosis (FISH analysis) of Prader-Willi syndrome
    • University Hospital Plovdiv - UMHAT Sv. Georgi - EAD
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • BULGARIA
    •  South Central region
    • PLOVDIV
    • Molecular diagnosis of Prader-Willi and Angelman syndromes (uniparental disomy or chromosome 15 deletion)
    • Université Saint-Joseph
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Deletion / Duplication analysis
    • More information
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • CHU d'Angers
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of male infertility with normal virilisation due to acquired testicular defect associated with mycoplasma infection
    • BIOAESIS
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • MARCHE
    • JESI
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome
    • Med-Biolog-Labor
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • KAISERSLAUTERN
    • Molecular diagnosis of Angelman and Prader-Willi syndrome by searching imprinting center defect of uniparental disomy
    • Istanbul Universitesi, Tip Fakültesi
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of Angelman and Prader-Willi syndrome by searching imprinting center defect of uniparental disomy
    • Istanbul Universitesi, Tip Fakültesi
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • 'Molecular diagnosis of Prader Willi Syndrome (15q11-13; deletion; UPD; methylation)'
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis, Deletion / Duplication analysis
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Cytogenetic diagnosis of Prader Willi (FISH and Molecular analysis)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Cytogenetic diagnosis of Prader Willi (FISH analysis)
    • The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Cytogenetic diagnosis of Prader Willi (FISH analysis)
    • Assaf Harofeh Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • ISRAEL
    • ISRAEL
    • BEER YAAKOV
    • Cytogenetic diagnosis of Prader-Willi syndrome (detection of microdeletions by FISH)
    • Centralny Szpital Kliniczny
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • POLAND
    • Lodz
    • LODZ
    • Prenatal and postnatal molecular cytogenetic diagnosis of Angelman and Prader-Willi syndrome (MLPA at 15q11)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of Prader-Willi and Angelman syndromes (microsatellite analysis)
    • Institute of Child Health
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of Prader-Willi syndrome (imprinting defects at 15q11-13)
    • Instytut "Pomnik-Centrum Zdrowia Dziecka"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome by FISH
    • Instytut "Pomnik-Centrum Zdrowia Dziecka"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of Prader-Willi syndrome by MLPA
    • Bioiatriki S.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome by FISH (SNRPN) analysis at 15q11-13
    • Complejo Hospitalario Universitario de Vigo. Hospital Xeral
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Galicia
    • VIGO
    • Molecular diagnosis of Prader-Willi (SNRPN gene)
    • University hospital Olomouc
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CZECH REPUBLIC
    • Olomouc
    • OLOMOUC
    • Molecular and molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Cytogenetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome
    • Azienda Ospedaliera "A. Cardarelli"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Diagnosis by FISH of Prader-Willi syndrome
    • GH du Havre - Hôpital Jacques Monod
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • LE HAVRE
    • Cytogenetic diagnosis of chromosomal microdeletion syndromes (FISH on blood, bone marrow, gonadal tissue and skin samples)
    • Szpital Uniwersytecki im. dr. Antoniego Jurasza
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • POLAND
    • Bydgoszcz
    • BYDGOSZCZ
    • Molecular cytogenetics diagnosis of Prader-Willi syndrome
    • Universitat Pompeu Fabra. Facultat de Ciències de la Salut i de la Vida
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of intellectual deficit syndromes (MLPA kits P064 & P096)
    • Instytut "Pomnik-Centrum Zdrowia Dziecka"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of microdeletions syndromes (MLPA kit P245 & P297)
    • Instytut "Pomnik-Centrum Zdrowia Dziecka"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of uniparental disomy (7, 14, 21 chromosomes)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene: MS-MLPA, MS-PCR/RFLP, allele specific REAL Time PCR, STR analysis of deletions)
    • University Hospital Bratislava - Stare mesto
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Deletion / Duplication analysis
    • Technical procedure(s) : PCR based techniques, MLPA based techniques
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of Prader-Willi Syndrome (methylation 15q11-q13)
    • Centralny Szpital Kliniczny
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • POLAND
    • Lodz
    • LODZ
    • Molecular diagnosis of Prader-Willi syndrome (SNRPN gene: MS-MLPA)
    • CHU Farhat Hached
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • TUNISIA
    • TUNISIA
    • SOUSSE
    • Molecular diagnosis of Prader Willi and Angelman syndromes (Methylation status of region 15q11.2)
    • Institut National d'Hygiène
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • MOROCCO
    • Rabat
    • RABAT
    • Molecular diagnosis of male infertility due to Y chromosome deletions (AZF)
    • Institut National d'Hygiène
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • More information
    • MOROCCO
    • Rabat
    • RABAT
    • Molecular diagnosis of Prader-Willi/Angelman syndrome (MS-MLPA-microduplications/microdeletions and methylation at 15q11/uniparental disomy of Chr15)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study, Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Prader-Willi syndrome (15q11-13, MS-MLPA)
    • Centro de estudios genéticos ATG Medical
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Uniparental disomy study
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Madrid
    • TRES CANTOS
    • Molecular cytogenetic diagnosis of Prader-Willi syndrome (FISH of SNRPN gene)
    • SELAS Arnaud-Biolys-Origet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • FRANCE
    • CENTRE
    • CHAMBRAY-LES-TOURS
    • Antenatal and postnatal molecular cytogenetic diagnosis of Prader-Willi/Angelman syndrome (determined by FISH)
    • Presidio Ospedaliero Centrale - Ospedale "San Marco"
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • ITALY
    • PUGLIA
    • GROTTAGLIE