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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of XX male syndrome by SRY gene study
    • LABOGEN S.a.S.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Accreditation
    • Molecular cytogenetic diagnosis of XX male syndrome
    • Medizinische Hochschule Hannover
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of microdeletions/microduplications
    • Technical procedure(s) : FISH
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular cytogenetic diagnosis of XX male syndrome (SRY gene)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular biology determination of SRY gene
    • CHU de LIEGE - UniLab Lg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Accreditation
    • Cytogenetic and molecular cytogenetic diagnosis of XX male syndrome (SRY gene)
    • Institut für Medizinische Genetik und angewandte Genomik Tübingen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of XX male syndrome (SRY gene)
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Accreditation
    • Molecular diagnosis of XX male syndrome (SRY gene)
    • Universitätsklinikum Ulm
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular cytogenetic diagnosis of XX male syndrome and XY Female type Gonadal Dysgenesis (SRY gene by FISH analysis)
    • St Mary's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of XX male syndrome (SRY gene)
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular biology determination of SRY gene
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular cytogenetic diagnosis of XX male syndrome
    • Institut für Humangenetik am Universitätsklinikum Jena
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Thüringen
    • JENA
    • Accreditation
    • Molecular diagnosis of Gonadal dysgenesis (SRY gene)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular cytogenetic diagnosis of XX male syndrome (SRY gene)
    • Institut für Klinische Genetik Mainz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • Molecular cytogenetic diagnosis of XX male syndrome and XY Female type Gonadal Dysgenesis (SRY gene by conventional karyotype and FISH analysis)
    • University Hospital of Wales
    • 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
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular and molecular cytogenetic diagnosis of SRY gene-associated disorders of sexual development
    • Medizinisches Versorgungszentrum Humane Genetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of SRY gene-associated diseases
    • MVZ Labor Dr. Reising-Ackermann und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • LEIPZIG
    • Accreditation
    • Molecular cytogenetic diagnosis of SRY gene-associated disorders of sexual development
    • Labor Lademannbogen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Determination of genetic sex in cases of sexual ambiguity (SRY gene)
    • Hôpitaux Universitaires de Genève HUG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis of SRY gene-associated diseases
    • Zentrum für Humangenetik Mannheim
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of SRY gene-associated diseases (sequencing, MLPA)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of 46,XX testicular disorder of sex development (SOX3, SOX9 genes)
    • Praxis für Humangenetik Freiburg
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Sex Determination For X-Linked Conditions For Disorders That Manifest Significantly Different In One Sex Compared To The Other by Targetted Mutation and Copy Number Analysis (Genes: AMELX, AMELY, SRY)
    • 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 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 SRY-Related Disorder of Sex Development (SRY del/dup)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Manitoba
    • WINNIPEG
    • Accreditation
    • Molecular diagnosis of SRY gene-associated diseases (sequencing)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Mutation analysis in SRY gene
    • Institut für angewandte Humangenetik und Onkogenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Accreditation
    • Molecular diagnosis of Gonadal Dysgenesis (sequence analysis of SRY plus diagnostic queries)
    • St James's University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • 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 SRY-Related Gonadal Disorder (mFISH SRY probe analysis)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • CANADA
    • Terre-Neuve-et-Labrador
    • ST. JOHN'S
    • Molecular diagnosis of gonadal dysgenesis (SRY gene)
    • Centre hospitalier intercommunal Poissy-Saint-Germain-en-Laye
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • POISSY
    • Molecular diagnosis of sexual ambiguity relatted to SRY gene
    • CHRU de Besançon - Hôpital Saint-Jacques
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • FRANCHE-COMTE
    • BESANÇON
    • Molecular diagnosis of gonadal dysgenesis (SRY gene)
    • Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular cytogenetic diagnosis of gonadal dysgenesis by SRY gene study
    • BIOS S.p.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Search for mutations in SRY gene
    • Centro de Análisis Genéticos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular cytogenetic diagnosis of XX male syndrome
    • Istituto CSS-Mendel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Cytogenetic and molecular diagnosis of XX male syndrome
    • CPSS - Centro Polidiagnostico Servizi Sanitari
    • 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
    • ITALY
    • SICILIA
    • CATANIA
    • Molecular cytogenetic diagnosis of XX male syndrome (SRY gene)
    • Institut für Humangenetik der Martin-Luther-Universität Halle Wittenberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Sachsen-Anhalt
    • HALLE (SAALE)
    • Cytogenetic and molecular cytogenetic diagnosis of XX male syndrome (SRY gene)
    • Universitätsklinikum Bonn
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular cytogenetics determination of SRY gene
    • Faculdade de Medicina da Universidade do Porto
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of 46,XX testicular disorder of sex development (SRY gene)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of gonadal dysgenesis (SRY gene)
    • Hospital Universitario Miguel Servet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Cytogenetic diagnosis of XX male syndrome
    • Toma Advanced Biomedical Assays S.p.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • ITALY
    • LOMBARDIA
    • BUSTO ARSIZIO
    • Cytogenetic diagnosis of XX male syndrome and XY Female type Gonadal Dysgenesis (SRY gene 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 XY gonadal dysgenesis (DHH, DMRT1, NR5A1, SRY genes)
    • Institut für Humangenetik des Universitätsklinikums Münster
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular cytogenetic diagnosis of 46,XX testicular disorder of sex development (SRY gene)
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Cytogenetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • 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 diagnosis of SRY-related developmental anomalies (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 diagnosis of SRY gene associated diseases
    • Toma Advanced Biomedical Assays S.p.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • BUSTO ARSIZIO
    • Molecular diagnosis of 45,X/46,XY mixed gonadal dysgenesis (search for SRY gene and entire coding sequence)
    • Lorgen G.P.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of sex determination disorders (SRY gene: analysis of coding region)
    • MEDGEN
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of 46,XY disorder of sex development (SRY, DHH, NR5A1, BMP15, FSHR genes)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular cytogenetics diagnosis of XX male syndrome (SRY gene / FISH)
    • Fundación Jiménez Díaz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of 46,XX testicular disorder of sex development (aCGH)
    • Genetadi Biotech S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular cytogenetic diagnosis of SRY-related developmental anomalies by FISH
    • Faculdade de Medicina da Universidade de Coimbra
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Technical procedure(s) : FISH
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular cytogenetics diagnosis of 46,XX testicular disorder of sex development (SRY gene, Yp11.31-p11.32 / 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 and cytogenetic diagnosis of sex differenciation anomalies and infertility (USP9Y and SRY genes)
    • Eurogenetica SA
    • 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
    • GREECE
    • GREECE
    • THESSALONIKI
    • Molecular diagnosis of disorders of sex development (SRY gene)
    • Instytut "Pomnik-Centrum Zdrowia Dziecka"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular Diagnosis of SRY-Related Disorder of Sex Development
    • CHU de Lyon HCL - GH Est
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), PCR based techniques
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Prenatal and postnatal molecular diagnosis of male sterility due to chromosome Y deletion (Y microdeletions in AZFa, AZFb, AZFc regions and SRY analysis by MLPA)
    • Laboratório de Análises Clínicas Dr. Joaquim Chaves
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • PORTUGAL
    • CENTRO
    • OEIRAS
    • Molecular diagnosis of SRY gene-associated diseases
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular cytogenetics diagnosis of XX male syndrome
    • Laboratori Campisi s.r.l.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • SICILIA
    • AVOLA
    • Molecular diagnosis of gonadal dysgenesia (SRY gene)
    • CHRU de Tours - Hôpital Bretonneau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • Molecular diagnosis of disorders of sex development/gonadal dysgenesis (SRY, HSD17B3, SRD5A2, NR5A1, WT1, FSHR gene)
    • Hospital Universitario Cruces - Osakidetza
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Molecular Cytogenetic Diagnosis of SRY-Related Gonadal Disorder (mFISH SRY 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
    • Diagnosis of 46,XX disorders of sex development (SOX9, WNT4, RSPO1 genes)
    • CHU de Lyon HCL - GH Est
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Molecular diagnosis of gonadal dysgenesis (SRY and NR5A1 genes)
    • CHRU de Montpellier - Hôpital Lapeyronie
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Molecular cytogenetics diagnosis of gonadal dysgenesis
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of XX male syndrome
    • Azienda Ospedaliera BMM
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CALABRIA
    • REGGIO CALABRIA
    • Analysis of the foetal DNA in the maternal blood : Search for sequences SRY (foetal sex) and RHD
    • CHU de Marseille - Hôpital Nord
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Molecular cytogenetics diagnosis of XX male syndrome
    • P.S.I. "Elena d'Aosta"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Cytogenetic diagnosis of XX male syndrome
    • Centro Associato "Pansini"
    • 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
    • MOLFETTA
    • Molecular cytogenetic diagnosis of XX male 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 XX male syndrome
    • Azienda Ospedaliera Ospedali Riuniti "Villa Sofia-Cervello" - Presidio Cervello
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • SICILIA
    • PALERMO
    • Cytogenetic diagnosis of XX male syndrome
    • Azienda Ospedaliera S. Anna
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • Objective(s) : Detection of chromosome alterations large in size
    • Technical procedure(s) : Karyotyping
    • More information
    • ITALY
    • LOMBARDIA
    • SAN FERMO DELLA BATTAGLIA
    • Search for mutations in SRY gene
    • Hospital Universitario de Canarias
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Canarias
    • SANTA CRUZ DE TENERIFE
    • Molecular cytogenetic diagnosis of XX male syndrome
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular cytogenetic diagnosis of XX male 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 XX male syndrome (SRY gene)
    • Associazione Cante di Montevecchio
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
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    • ITALY
    • MARCHE
    • FANO
    • Molecular cytogenetic diagnosis of XX male syndrome
    • Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
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    • ITALY
    • FRIULI VENEZIA GIULIA
    • UDINE
    • Cytogenetic and molecular diagnosis of XX male syndrome
    • IRCCS Arcispedale Santa Maria Nuova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
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    • ITALY
    • EMILIA ROMAGNA
    • REGGIO EMILIA
    • Molecular cytogenetic diagnosis of XX male syndrome
    • Casa di Cura "Città di Udine"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • UDINE
    • Molecular cytogenetic diagnosis of XX male syndrome (SRY gene)
    • Praxis Dr. med. Ulrike Beudt
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
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    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • 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
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    • ITALY
    • MARCHE
    • JESI
    • Molecular diagnosis of 46,XX testicular disorder of sex development (SRY)
    • Wolfson Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
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    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular cytogenetics diagnosis of XX, male syndrome
    • Azienda Ospedaliera Universitaria "Federico II"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Cytogenetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • SRY gene molecular cytogenetics analysis for 46, XX testicular disorder of the sex development, bilateral anorchidia, gonadal dysgenesis XY female type and XY/XO gonadal dysgenesis. FISH analysis
    • 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 46,XX testicular disorder of sex development (SRY gene)
    • Hospital San Pedro
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
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    • SPAIN
    • La Rioja
    • LOGROÑO
    • 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
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    • MOROCCO
    • Rabat
    • RABAT