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Caption : Accreditation =Accreditation
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    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Molecular diagnosis of microdeletion syndromes (array-CGH)
    • CHU de Nice - Hôpital l'Archet 2
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • BOIS-GUILLAUME
    • Accreditation
    • FISH anlyses of microdeletions / microduplications
    • Etablissement français du sang - Normandie
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis (MLPA) of 22q13.3 microdeletion
    • Centre Médical Universitaire - CMU
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Diagnosis of microdeletion and microduplication syndromes by array CGH
    • Ruhr-Universität Bochum
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Accreditation
    • Molecular cytogenetic diagnosis of deletion 22q13
    • Institut für angewandte Humangenetik und Onkogenetik
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular cytogenetic diagnosis of deletion 22q13.2
    • Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Diagnosis of microdeletion and microduplication syndromes by array CGH
    • Medizinisches Versorgungszentrum Humane Genetik
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of deletion 22q13 (FISH and MLPA)
    • Medizinisches Versorgungszentrum Humane Genetik
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Diagnosis of microdeletion and microduplication syndromes by FISH and array CGH
    • Medizinisch Genetisches Zentrum München
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular cytogenetics diagnosis of 22q13.3 microdeletion (FISH; array-CGH)
    • Universität Zürich
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Accreditation
    • Molecular and Cytogenetic diagnosis of Chromosomal Anomalies (Karyotyping, SNP-Array and FISH)
    • Ghent University Hospital - UZGent
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular cytogenetics diagnosis(FISH) of 22 q13.3 microdeletion
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Microdeletion screening by MLPA
    • Universität Würzburg - Biozentrum
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular cytogenetic diagnosis of Monosomy 22q13 (Phelan-McDermid syndrome, by FISH analysis)
    • Birmingham Women's NHS Foundation Trust
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of deletion 22q13 (MLPA: SHANK3, ACR, RABL2B genes)
    • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular cytogenetics diagnosis of 22q13 deletion
    • Universität Zürich
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular cytogenetic diagnosis of Deletion 22q13.3 (by FISH analysis)
    • St Mary's Hospital
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular and cytogenetic diagnosis of Chromosomal Anomalies (Karyotyping, SNP-Array and FISH)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular cytogenetic diagnosis of 22q13 microdeletion (FISH analysis)
    • Southmead Hospital
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular cytogenetic diagnosis of Deletion 22q13.3 (by conventional karyotype and FISH analysis)
    • University Hospital of Wales
    • More information
    • CANADA
    • Québec
    • MONT-ROYAL, MONTRÉAL
    • Accreditation
    • Diagnosis of microdeletion and microduplication syndromes by array analysis
    • PROCREA Cliniques
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Preimplantation molecular cytogenetic diagnosis of chromosomal anomalies, X-linked diseases and aneuploidy screening (by FISH or array CGH)
    • Institute for Women's Health
    • More information
    • FRANCE
    • BRETAGNE
    • RENNES
    • Postnatal diagnosis of microdeletions and microduplications (by array-CGH)
    • CHU de Rennes - Hôpital Pontchaillou
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Array-CGH analyses of microdeletions and microduplications
    • CHU de Nantes - Institut de Biologie
    • More information
    • FRANCE
    • OUTRE-MER
    • SAINT-DENIS
    • FISH analysis of microdeletions / microduplications
    • CHU de la Réunion - Hôpital Félix Guyon
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Preimplantation and postnatal cytogenetic diagnosis of deletion 22q13 (FISH analysis)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Search for subtelomeric rearrangements by MLPA (P036 & P070 kits)
    • CHU Paris - Hôpital Robert Debré
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Search for recurrent chromosomal rearrangements by MLPA (P245 & P297 kits)
    • CHU Paris - Hôpital Robert Debré
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular cytogenetics diagnosis of 22q13 deletion
    • CHU Paris Centre - Maternité Port Royal
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of microdeletion/ microduplication syndromes (by array)
    • CHU Paris Centre - Maternité Port Royal
    • More information
    • FRANCE
    • LIMOUSIN
    • LIMOGES
    • Molecular cytogenetics diagnosis of microdeletion microduplication syndromes (caryotype, FISH)
    • CHU de Limoges - Hôpital de la mère et de l'enfant
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Prenatal diagnosis of microdeletions and microduplications (array-CGH)
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Molecular cytogenetic analysis of microdeletions/microduplications (by FISH)
    • CHU de Grenoble site Nord - Hôpital Couple-Enfant
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Cytogenetics molecular diagnosis of monosomy 22q13.3
    • Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetic diagnosis of deletion 22q13.3
    • Istituto CSS-Mendel
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of monosomy 22q13 (SHANK3 gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Diagnosis of microdeletion and microduplication syndromes by array CGH
    • Praxis für medizinische Genetik
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Diagnosis of microdeletion and microduplication syndromes by array CGH
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of microdeletions syndromes (MLPA kit P245)
    • Policlínica Gipuzkoa
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of deletion 22q13.3 syndrome (array-CGH)
    • Policlínica Gipuzkoa
    • More information
    • SPAIN
    • Baleares
    • PALMA DE MALLORCA
    • Molecular diagnosis of microdeletion syndromes by MLPA (kit P245)
    • Hospital Universitario Son Espases
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular cytogenetics diagnosis of monosomy 22q13 (detection of 22q13 deletion)
    • Hospital Universitario Virgen del Rocío
    • More information
    • FRANCE
    • AUVERGNE
    • CLERMONT-FERRAND
    • FISH analysis of microdeletions / microduplications
    • CHU de Clermont-Ferrand - Hôpital d'Estaing
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of chromosomal abnormalities (array-CGH)
    • CIC - Centro de Investigación del Cáncer
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular cytogenetic diagnosis of Phelan-Mcdermid syndrome (22q13.3): FISH/MLPA.
    • Faculdade de Medicina da Universidade do Porto
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of monosomy 22q13 (MLPA)
    • Hospital Universitario Miguel Servet
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of monosomy 22q13 (SHANK3 gene)
    • Fundación Jiménez Díaz
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of Phelan-McDermid syndrome (MLPA)
    • Leto Maternity Hospital
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of monosomy 22q13 by MLPA
    • Mitera General, Maternity and Children's Hospital
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular cytogenetic diagnosis of Phelan-Mcdermid syndrome by FISH analysis
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Phelan-McDermid syndrome (SHANK3 gene: deletion/duplication analysis)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Preimplantation genetic diagnosis of chromosomal anomalies
    • Reprogenetics Spain S.A.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular cytogenetics diagnosis of monosomy 22q13: diagnostic and prenatal testing (FISH 22q11.2/22q13)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Molecular cytogenetic diagnosis of deletion 22q13
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Cytogenetic diagnosis of Deletion 22q13.3 (by conventional karyotype and FISH analysis)
    • Cambridge University Hospitals NHS Foundation Trust
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Diagnosis of microdeletion and microduplication syndromes by array CGH
    • Universitätsklinikum Bonn
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Diagnosis of microdeletion and microduplication syndromes by array CGH
    • Institut für Klinische Genetik Bonn
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • MLPA analysis of microdeletion syndrome regions
    • Universitätsmedizin Mainz
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Cytogenetic diagnosis of Monosomy 22q13 (Phelan-McDermid syndrome, by FISH at 22q13.33)
    • Guy's Hospital
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of Phelan-McDermid syndrome by MLPA
    • Bioiatriki S.A.
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular cytogenetic diagnosis of monosomy 22q13 (FISH analysis)
    • CHRU de Brest - Hôpital Morvan
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Molecular cytogenetic diagnosis of 22q deletion syndrome (FISH analysis)
    • St George's University of London
    • More information
    • POLAND
    • Warszawa
    • WARSZAWA
    • Cytogenetic diagnosis of constitutional chromosomal abnormalities (microdeletion/ microduplication syndromes by FISH, MLPA, array CGH: MLPA kits P245, P297, P036)
    • Instytut Matki i Dziecka
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular cytogenetic diagnosis of Phelan-Mcdermid syndrome by FISH
    • Faculdade de Medicina da Universidade de Coimbra
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular diagnosis of microdeletion syndromes (by MLPA kit P297 & P245)
    • Faculdade de Medicina da Universidade de Coimbra
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular diagnosis of mental retardation and autism by array-CGH
    • Faculdade de Medicina da Universidade de Coimbra
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular and molecular cytogenetics diagnosis of chromosomal anomalies (array-CGH and FISH)
    • Hospital Clínic de Barcelona
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of 22q13 deletion syndrome: diagnostic and prenatal testing (locus 22q13 / MLPA)
    • Hospital Clínico San Carlos
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Preimplantation molecular cytogenetic diagnosis of chromosomal anomalies (FISH)
    • Igenomix Spain
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Cytogenetics pre-natal and post-natal diagnosis of monosomy 22q13 (by FISH)
    • CHRU de Montpellier - Hôpital Arnaud de Villeneuve
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Pre-natal and post-natal diagnosis of microdeletions/microduplications by array-CGH
    • CHRU de Montpellier - Hôpital Arnaud de Villeneuve
    • More information
    • FRANCE
    • ALSACE
    • STRASBOURG
    • Molecular diagnosis of microdeletions / microduplications by CGH arrays
    • CHU de Strasbourg - Hôpital de Hautepierre
    • More information
    • FRANCE
    • BRETAGNE
    • RENNES
    • Prenatal diagnosis of microdeletions and microduplications (Array-CGH)
    • CHU de Rennes - Hôpital Pontchaillou
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • BONDY
    • Cytogenetic and molecular diagnosis of mocrodeletional syndromes chromosomal desequilibrium (FISH and CGH arrays analysis)
    • CHU Paris Seine-Saint-Denis - Hôpital Jean Verdier
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular diagnosis of deletion 22q13.3
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular cytogenetics diagnosis of deletion 22q13.3
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetic diagnosis of developmental anomalies (CGH Array)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular cytogenetics diagnosis of monosomy 22q13 syndrome
    • Azienda Ospedaliera Universitaria "Federico II"
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetic diagnosis of deletion 22q13
    • Policlinico Universitario "A. Gemelli"
    • More information
    • ITALY
    • ABRUZZO
    • L'AQUILA
    • Molecular cytogenetic diagnosis of 22q13.3 deletion
    • Università degli Studi dell'Aquila - Coppito
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular cytogenetic diagnosis of deletion 22q13
    • Institut für Humangenetik der LMU-München
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BASEL
    • Molecular cytogenetics diagnosis (FISH) of 22q13.3 microdeletion
    • University Children's Hospital - UKBB
    • More information
    • ITALY
    • LOMBARDIA
    • BOSISIO PARINI
    • Molecular cytogenetic diagnosis of deletion 22q13.3 (SHANK3 gene)
    • IRCCS "E. Medea"
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • REGGIO EMILIA
    • Molecular cytogenetic diagnosis of deletion 22q13.3
    • IRCCS Arcispedale Santa Maria Nuova
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular cytogenetic diagnosis of monosomy 22q13 (SHANK3 gene)
    • Institut für Humangenetik am Universitätsklinikum Freiburg
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Molecular cytogenetic diagnosis of deletion 22q13
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • ITALY
    • UMBRIA
    • PERUGIA
    • Molecular cytogenetic diagnosis of monosomy 22q13
    • Azienda Ospedaliera Universitaria di Perugia Santa Maria della Misericordia
    • More information
    • SPAIN
    • Galicia
    • VIGO
    • Molecular cytogenetics diagnosis of deletion 22q13 by FISH analysis (ARSA)
    • Complejo Hospitalario Universitario de Vigo - Hospital Xeral
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • NEUILLY-SUR-SEINE
    • Molecular cytogenetic diagnosis of microdeletion syndromes
    • Laboratoire d'Eylau
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular cytogenetic diagnosis of deletion 22q (by FISH)
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • More information
    • POLAND
    • Bydgoszcz
    • BYDGOSZCZ
    • Cytogenetic diagnosis of chromosomal microdeletion syndromes (FISH on blood, bone marrow, gonadal tissue and skin samples)
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular cytogenetic diagnosis of monosomy 22q13 by FISH
    • The Children's Memorial Health Institute CMHI (IP-CZD)
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of microdeletions syndromes (MLPA kit P245 & P297)
    • The Children's Memorial Health Institute CMHI (IP-CZD)
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of monosomy 22q13 (aCGH)
    • Genetadi Biotech S.L.
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular cytogenetics and molecular diagnosis of monosomy 22q13 (array CGH, FISH, MLPA)
    • Hospital Universitari General Vall d'Hebron
    • More information