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188 Result(s)

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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 and GJB6 genes)
    • Laboratoire Cerba
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • SAINT-OUEN-L'AUMÔNE
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Ruhr-Universität Bochum
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für Humangenetik der Universität Göttingen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Paxis und Labor Dr. med Karl Mehnert
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (COCH and GJB2, 3, and 6 genes)
    • Medizinische Universität Innsbruck
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Accreditation
    • Molecular diagnosis of deafness nonsyndromic (GJB2, GJB6 genes)
    • Hôpitaux Universitaires de Genève HUG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis of Autosomal dominant nonsyndromic sensorineural deafness, DFNA9 (COCH gene (P51S))
    • University Hospitals Leuven - Gasthuisberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of autosomal dominant nonsyndromic genetic deafness (WFS1 and COCH genes)
    • 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 diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • 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 deafness due to connexin 26 anomaly
    • Erasme Hospital - ULB
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Mitteldeutscher Praxisverbund Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of Non-syndromic Deafness (GJB2 & GJB6 genes)
    • Ninewells Hospital and Medical School
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Accreditation
    • Molecular diagnosis of deafness due to Connexin 26 anomaly (GJB2 gene)
    • Great Ormond Street Hospital for Children, York House
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Medizinische Versorgungszentrum Dr.Stein + Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÖNCHENGLADBACH
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3 and GJB6 genes)
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of Nonsyndromic genetic deafness (GJB2 and GJB6 genes)
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Autosomal dominant non-syndromic sensorineural deafness type DFNA (COCH gene, p. P51S mutation)
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Nonsyndromic Hearing Loss and Deafness due to connexin 26 anomaly (GJB2 gene)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of non syndromic hearing loss and deafness DFNA9 (COCH gene)
    • Inselspital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BERN
    • Accreditation
    • Molecular diagnosis of Autosomal Dominant Deafness (DIAPH1, KCNQ4, GJB2, GJB6, DFNA5, WFS1, TECTA, COCH, EYA4, MYO7A, COL11A2, POU4F3, MYH9, ACTG1 and MYO6 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3, GJB6, MYH9, SLC26A4 genes)
    • Praxis für Humangenetik Freiburg
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of sensorineural deafness DFNA17 (MYH9 gene)
    • Praxis Dr. Mato Nagel
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Accreditation
    • Molecular diagnosis of non syndromic sensorineural deafness (GJB2, GJB3, GJB6, MYO7A, MYO15A, SLC26A4, SLC26A5, TMC1, MT-RNR1 and MT-TS1 genes : APEX, total sequencing ; GJB2 gene : exon 1 donor splice junction sequencing)
    • Asper Biotech Ltd.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (MYH14, WFS1 genes)
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB6, MYH9, MYO7A, SIX1, SLC26A4 genes)
    • Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of autosomal dominant non syndromic sensorineural deafness (CCDC50, COCH , COL11A2, DIAPH1, DFNA5, EYA4, GJB2, GJB3, GJB6, HGF, KCNQ4, MYH9, MYH14, MYO6, MYO7A, POU4F3, SIX1, TECTA, TMC1, WFS1 genes)
    • Centogene AG
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsklinikum Ulm
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular screening of frequent diseases in Ashkenazi Jewish populations (APEX: ABCC8, AGL, ASPA, BCKDHB, BLM, CFTR, CLRN1, DLD, F11, FANCC, G6PC, GBA, GJB2, HEXA, IKBKAP, LDLR, MCOLN1, MEFV, NEB, PCDH15, SERPINA1, SMPD1, TMEM216 and TOR1A genes)
    • Asper Biotech Ltd.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsmedizin Mainz
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes: sequencing, MLPA)
    • Zentrum für Humangenetik Mannheim
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Labor Lademannbogen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of congenital deafness (GJB2 &GJB6 genes)
    • 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 autosomal dominant non syndromic sensorineural deafness (ACTG1, CCDC50, COCH, COL11A2, DIAPH3, DFNA5, DIAPH1, EYA4, GJB2, GJB3, GJB6, KCNQ4, MIRN96, MYH14, MYH9, MYO1A, MYO6, MYO7A, POU4F3, SLC17A8, TECTA, TFCP2L3, TMC1, WFS1, HGF genes: sequencing, linkage analysis)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3, GJB6, STRC genes)
    • Universität Würzburg - Biozentrum
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • GHU Paris-Sud - Hôpital de Bicêtre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICÊTRE
    • Accreditation
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness (GJB2 and GJB6 genes)
    • Genetica AG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJA1, GJB2 and GJB6 genes: sequencing, MLPA)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • 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
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of nonsyndromic sensorineural dafness (GJB2 gene)
    • LABOGEN S.a.S.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Accreditation
    • Molecular diagnosis of Autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2 and GJB6 genes)
    • 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 autosomal dominant non-syndromic sensorineural deafness type DFNA (GJB2, GJB3, GJB6, MYH9, TECTA, WFS1 genes)
    • CeGaT GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Deafness (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES), Whole Exome Sequencing (WES)
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness, dominant or recessive (GJB2 gene)
    • Complejo Asistencial Universitario de Salamanca
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinische Universität Graz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Accreditation
    • Molecular diagnosis of non-syndromic sensorineural deafness (GJB2, GJB3, GJB6 and WFS1 genes: sequencing of entire coding region and delection analysis by MLPA)
    • Instituto de Biologia Molecular e Celular
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : MLPA based techniques
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Accreditation
    • Molecular diagnosis of non-syndromic congenital deafness (GJB6, SLC26A4, OTOF genes: Sequencing of entire coding region)
    • Instituto de Biologia Molecular e Celular
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB6 and SLC26A4 genes: sequencing / MLPA)
    • GenteQ 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
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (COCH gene exons 4 and 5 ; WFS1 gene exon 8 ; TECTA, KCNQ4 genes)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB6, OTOF genes)
    • Pränatalmedizin München
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular Diagnosis of GJB2-related Sensorineural Hearing Loss (GJB2 sequencing)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Manitoba
    • WINNIPEG
    • Accreditation
    • Molecular Diagnosis of GJB6-related Sensorineural Hearing Loss (GJB6 sequencing)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Manitoba
    • WINNIPEG
    • Accreditation
    • Molecular diagnosis of nonsyndromic deafness (GJB2 entire coding region)
    • Universität Zürich
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular Diagnosis of Hereditary Hearing Loss: Nonsyndromic/Common HL NGS Panel and Del/Dup Analysis (59 genes including MIR18S, MIR183)
    • The Hospital for Sick Children and University of Toronto
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), Array based techniques
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molekulare Diagnostik der sensorineuralen Schwerh÷rigkeit (GJB2- und GJB6-Gen)
    • Labor PD Dr. Volkmann und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Diagenom GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Antenatal and postnatal molecular diagnosis of non-syndromic sensorineural deafness (sequence analysis of the entire coding region and selected exons, mutation scanning of selected exons and the entire coding region of GJB2 and GJB6 genes)
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für angewandte Humangenetik und Onkogenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für Laboratoriumsmedizin und Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • SINGEN /HTWL.
    • Accreditation
    • Molecular Diagnosis of Nonsyndromic Hearing Loss (GJB2 c.35delG mutation)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Terre-Neuve-et-Labrador
    • ST. JOHN'S
    • Accreditation
    • Molecular Diagnosis of Non-syndromic Genetic Deafness (GJB2, GJB6 NGS)
    • London Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • CANADA
    • Ontario
    • LONDON
    • Molecular diagnosis of genetic nonsyndromic deafness: search for mutations of GJB2, GJB3 and GJB6 genes
    • CHU de Bordeaux-GH Pellegrin
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of non syndromic genetic deafness (GJB2, GJB6, TECTA, MYO15A, OTOF, TMC1, MT-RNR1, CEACAM16, COCH, DIAPH1, DIAPH3, MYH9, POU4F3, TJP2, CLDN14, MYO6, SLC26A4, SMPX genes; NGS)
    • IURC - Institut Universitaire de Recherche Clinique
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Molecular diagnosis of non syndromic deafness (GJB2, GJB6 genes)
    • CHRU de Brest - Hôpital Morvan
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular diagnosis of deafness due to connexin types (GJA1,GJB6,GJB2 genes)
    • Ospedali Galliera
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of connexin 26 deafness (GJB2 gene)
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Istituto CSS-Mendel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 and 30 deafness (GJB6-D13S80)
    • Ospedale Maggiore Policlinico - Clinica Mangiagalli
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2, GJB6 genes)
    • Laboratorio Genoma
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Humangenetisches Institut am Universitätsklinikum Erlangen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • ERLANGEN
    • Molecular diagnosis of connexin 26 linked nonsyndromic deafness
    • Gemeinschaftspraxis Dres. Algermissen / Justus / Wilke / Graf
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Niedersachsen
    • HILDESHEIM
    • Molecular diagnosis of non-syndromic deafness (GJA1, GJB2, GJB3, GJB6 and MT-RNR1 genes)
    • Ospedale Regionale per le Microcitemie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Molecular diagnosis of connexin 26 anomaly
    • Centro de Análisis Genéticos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of non-syndromic deafness (GJB2, GJB6 genes)
    • Azienda Ospedaliera di Padova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of non syndromic deafness due to connexines 26 and 30 (GJB2, GJB 6 genes)
    • 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 diagnosis of non syndromic deafness due to connexin anomalies (GJB2, GJB6 genes)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of non syndromic deafness due to connexin 26 anomaly (GJB2, GJB6 genes)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness (GJB2, GJB6 genes)
    • CHRU de Lille - Centre de Biologie Pathologie Génétique
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of sensorineural deafness (GJB2 gene sequencing)
    • Turku University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of sensorineural deafness: sequencing of the GJB2 gene
    • Oulu University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FINLAND
    • Finland
    • OULU
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Molecular diagnosis of deafness nonsyndromic sensorineural (GJB2, GJB3, GJB6, GJA1, SLC26A4, and SLC26A5 genes)
    • Tartu University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Molecular diagnosis of autosomal dominant non-syndromic sensorineural deafness type DFNA due to connexin 26 and 30 anomaly (GJB2 and GJB6 genes)
    • CHU de Reims - Hôpital Maison Blanche
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praxis Dres. Gencik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of connexin 26 and 30 anomalies (GJB2 and GJB6 genes)
    • Diagnostic Genetic Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Full mutation analysis via sequencing of deafness due to connexin 26 (GJB2 gene 13q12.11)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Molecular diagnosis of deafness, nonsyndromic sensorineural recessive (GJB2, GJB3 and GJB6 genes: Analysis of the entire coding region - Sequence analysis)
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of non syndromic deafness due to connexines 26 and 30 anomaly (GJB2 and GJB6 genes)
    • B.I.R.D. Foundation
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für Humangenetik am Universitätsklinikum Köln
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • Gennet s.r.o.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • Genexpress Ltd.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of nonsyndromic genetic deafness by PCR-RFLP (GJB2 gene)
    • Semmelweis University Hospital - 2nd Department of Paediatrics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : PCR based techniques
    • More information
    • HUNGARY
    • Közép-Magyarország
    • BUDAPEST
    • Molecular diagnosis of genetic nonsyndromic deafness, due to connexin 26 anomalies (GJB2 gene)
    • CPSS - Centro Polidiagnostico Servizi Sanitari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3 and GJB6 genes)
    • Institut für Humangenetik des Universitätsklinikums Münster
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of non syndromic deafness due to connexin 26 anomalies (CX26 gene)
    • Consorzio per la Genetica Molecolare Umana
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MONZA
    • Molecular diagnosis of nonsyndromic hereditary deafness due to connexin 26 anomalies
    • Karolinska University Hospital - Solna
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of Congenital hearing-loss (GJB2 gene)
    • University Medical Centre Ljubljana
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SLOVENIA
    • SLOVENIA
    • LJUBLJANA
    • Molecular diagnosis of non syndromic genetic deafness (frequent deletions in GJB2 and GJB6 genes detected by MLPA)
    • Sygehus Lillebaelt Vejle Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • DENMARK
    • Syddanmark
    • VEJLE
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • Clinical Center - University of Pécs
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • HUNGARY
    • Dél-Dunántúl
    • PECS
    • Molecular diagnosis of sensorineural deafness (GJB1, GJB2, GJB3, GJB4 and GJB6 genes: sequencing, MLPA)
    • bio.logis Zentrum für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinisches Versorgungszentrum
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • NÜRNBERG
    • Molecular diagnosis of nonsyndromic genetic deafness (GJB2, GJB6 and OTOF genes)
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of genetic deafness
    • Tecnobios Prenatale S.r.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • Genetiks - Genetic diagnosis and research center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of nonsyndromic genetic deafness
    • Maribor general hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SLOVENIA
    • SLOVENIA
    • MARIBOR
    • Molecular diagnosis of non syndromic deafness due to connexin 26 (CX26 gene)
    • GENETICLAB Srl
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • VENETO
    • NOVENTA VICENTINA
    • Molecular diagnosis of autosomal dominant non syndromic genetic deafness (GJB2 and GJB6 genes)
    • CHU de Lyon HCL - GH Est
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für Klinische Genetik Bonn
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Praxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bremen
    • BREMEN
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB3, MYH14, EYA4, MYO7A, TECTA, COL11A2, MYH9, MYO6, TMC1, MYO1A, GRHL2 genes)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness type DFNA and DFNB (GJB2 and GJB6 genes)
    • Faculdade de Medicina da Universidade de Lisboa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • MVZ Humangenetik Ulm
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Klinikum Stuttgart - Standort Olgahospital
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (COCH, EYA4, GJB2, GJB3, GJB6, TECTA genes)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of sensorineural deafness (GJB6 gene: hotspot)
    • Praxis für Humangenetik und Prävention
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of sensorineural deafness (COL11A2, GJB2,GJB6, TECTA genes)
    • Gemeinschaftspraxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Antenatal and postnatal molecular diagnosis of nonsyndromic sensorineural deafness (targeted mutation analysis of GJB2, GJB6 genes)
    • ASLRM1 - Centro per la tutela della Salute della Donna e del Bambino
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of nonsyndromic deafness (GJB2, MT-RNR genes)
    • Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB6 genes)
    • Biotecnologie Avanzate Srl
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of non-syndromic, autosomal recessive, dominant and X-linked hearing loss (GJB6, GJB2, GJB3, POU3F4, WFS1 genes: deletion/duplication analysis by MLPA (kit P163))
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinische Universität Wien
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes: sequencing)
    • Institut für Humangenetik am Universitätsklinikum Freiburg
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praenatal-Medizin und Genetik, Düsseldorf
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Laborärztlich-humangenetische Partnerschaft Eiben - Glaubitz
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2, GJB6 genes)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness (GJB2 gene)
    • Eurogenetica SA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GREECE
    • GREECE
    • THESSALONIKI
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2 gene)
    • Hospital Universitario Puerta del Mar
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • CÁDIZ
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2, GJB6 genes / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of non syndromic genetic deafness - Connexin 26 and 30 (GJB2 gene/sequencing, complete coding regions + GJB6 gene/mutation 309kb del(GJB6-D13S1830) + 232kb del(GJB6-D13S1854))
    • Montreal Children's hospital - Hôpital de Montréal pour enfants
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Molecular diagnosis of macrothrombocytopenia and progressive sensorineural deafness (MYH9 gene: sequencing of entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB6 gene / sequencing)
    • Universidad de Salamanca. Facultad de Medicina
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2 gene / sequencing)
    • Instituto Bernabeu Biotech
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ALICANTE
    • Molecular diagnosis of connexin 26 and 30 deafness (GJB2, GJB6 genes)
    • Laboratori Campisi s.r.l.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • AVOLA
    • Molekulare Diagnostik der sensorineuralen Schwerh÷rigkeit (GJB2- und GJB6-Gen)
    • UKE - Universitätsklinikum Hamburg-Eppendorf
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Molecular diagnosis of genetic deafness (GJB2, GJB3, GJB6, WFS1, POU3F4 genes / PCR, gene sequencing, MLPA, capillary electrophoresis; OTOF, COCH , SLC26A4, PAX3, MT-RNR1, MT-TL1, MT-TS1 genes / PCR, exons sequencing)
    • IMOMA - Instituto de Medicina Oncológica y Molecular de Asturias
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : PCR based techniques, MLPA based techniques
    • More information
    • SPAIN
    • Asturias
    • OVIEDO
    • Molecular Diagnosis of Non-Syndromic Sensorineural Hearing Loss (GJB2 sequencing, GJB6 targeted mutation analysis)
    • BC Women's Hospital and Health Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • Molecular diagnosis of connexin-related non-sydromic deafness (GJB6 and GJB2 genes by PCR and agarose gel electrophoresis; sequencing of GJB2 gene)
    • Centro Interdipartimentale per la Biologia Integrata (CIBIO)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : PCR based techniques
    • More information
    • ITALY
    • TRENTINO ALTO ADIGE
    • MATTARELLO
    • Molecular diagnosis of genetic deafness (amplification of 1-464 region in CX26 gene determined by PCR)
    • TEST s.r.l.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : PCR based techniques
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • MODENA
    • Molecular diagnosis of non-syndromic sensorineural deafness associated to connexin 26 and 30 deafness (CX26 and CX30 genes)
    • RDI - RETE DIAGNOSTICA ITALIANA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • VENETO
    • LIMENA
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Praxis für Humangenetik Dr. Lemmens
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • AACHEN
    • Molekulare Diagnostik der sensorineuralen Schwerh÷rigkeit (GJB2- und GJB6-Gen)
    • MVZ wagnerstibbe für Laboratoriumsmedizin und Pathologie GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Institut für Humangenetik am Universitätsklinikum Leipzig
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • LEIPZIG
    • Analysis of known mutation for deafness due to connexin 26 (GJB2 gene 13q12.11)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Deletion analysis of deafness due to connexin 30 (GJB6 gene 13q12.11 / GJB6-D13S1830)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • DNA storage/extraction of GJB2 and GJB6 for deafness due to connexin 26 and connexin 30 (GJB2 gene 13q12.11 and GJB6 gene 6p31.23)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praxis für Humangenetik und Prävention
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Postnatal molecular diagnosis of autosomal dominant non-syndromic sensorineural deafness type DFNA (determined by Sanger sequencing and NGS)
    • Azienda Ospedaliera di Padova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Diagnosis of autosomal non-syndromic sensorineural deafness (GJB2 and GJB6 genes)
    • CHU Paris IdF Ouest - Hôpital Ambroise Paré
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • BOULOGNE-BILLANCOURT
    • Molecular diagnosis of connexin 26 deafness (GJB2 gene)
    • Centro Medico Artemisia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • BIOS S.p.A.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 and 30 deafness (GJB2, GJB6 genes)
    • IRCCS Burlo Garofolo - Istituto per l'Infanzia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • TRIESTE
    • Molecular diagnosis of nonsyndromic deafness due to connexin anomalies 26, 30 and 31
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of connexines 26, 30 and 31 anomaly (GJB2, GJB3 and GJB6 genes)
    • Policlinico Universitario "A. Gemelli"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Fondazione IRCCS Policlinico San Matteo
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • PAVIA
    • Molecular diagnosis of connexin 26 and 30 anomaly (GJB2 and GJB6 genes)
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of nonsyndromic genetic deafness (GJB2 and GJB6 genes)
    • HUMV - Hospital Universitario Marqués de Valdecilla
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cantabria
    • SANTANDER
    • Molecular diagnosis of congenital deafness (GJB2 gene)
    • Complejo Hospitalario Universitario Insular-Materno Infantil
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Canarias
    • LAS PALMAS DE GRAN CANARIA
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJA1, GJB2, GJB3, GJB6, MIR96 genes)
    • A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • VARESE
    • Molecular diagnosis of connexin 26 and 30 anomalies and genetic deafness (GJB2 and GJB6 genes)
    • Ospedale Niguarda Ca' Granda
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of connexines 26 and 30 anomalies
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular diagnosis of deafness, neurosensory (connexin 26 and 30)
    • Allgemeines Krankenhaus der Stadt Wien
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Prenatal and postnatal molecular diagnosis of non-syndromic hearing impairement (GJB2 and GJB6 mutation screening)
    • Mitera General, Maternity and Children's Hospital
    • Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Associazione Cante di Montevecchio
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • MARCHE
    • FANO
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • USI - Unione Sanitaria Internazionale
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • University hospital Brno
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CZECH REPUBLIC
    • South Moravia
    • BRNO
    • Molecular diagnosis of genetic nonsyndromic deafness (GJB2 and GJB6 genes)
    • Presidio Ospedaliero "Madonna delle Grazie" - Azienda Sanitaria di Matera (ASM)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • BASILICATA
    • MATERA
    • Molecular diagnosis of nonsyndromic deafness due to connexin 26 anomaly
    • Università degli Studi di Perugia - Ospedale S. Maria della Misericordia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • UMBRIA
    • PERUGIA
    • Molecular diagnosis of neurosensorial deafness (GJB2 gene)
    • Policlinico Universitario di Chieti
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • ABRUZZO
    • CHIETI
    • Molecular diagnosis of nonsyndromic hereditary deafness due to connexin 26, 30, 31, 32 and 43 anomalies
    • GENICA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BULGARIA
    •  South-West region
    • SOFIA
    • Molecular diagnosis of Non-syndromic hearing loss (GJB2, GJB6, Mutation analysis)
    • Wolfson Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular diagnosis of non syndromic genetic deafness (complete GJB2 gene sequencing)
    • Université Saint-Joseph
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Molecular diagnosis of non syndromic deafness due to connexines 26 and 30 (GJB2 and GJB6 genes)
    • Università degli Studi di Brescia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • BRESCIA
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene sequencing and detection of common mutations)
    • Institute of Child Health
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of nonsyndromic genetic deafness (GJB2 and GJB6 genes)
    • Warszawski Uniwersytet Medyczny
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of deafness, autosomal dominant, nonsyndromic, sensorineural, type DFNA (MYH9, ACTG1, COL11A2, CCDC50, DFNA5, KCNQ4 , DIAPH1, EYA4, POU4F3, GJB2, GJB6, TMC1, MYH14, TECTA, WFS1, MIR96, COCH genes)
    • Hospital Universitario Ramón y Cajal
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • Laboratory of Forensic Genetics, Laborator forenzni genetiky, spol. s r.o.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CZECH REPUBLIC
    • Moravia-Silesia
    • OSTRAVA-PORUBA
    • Molecular diagnosis of nonsyndromic sensorineural deafness, autosomal dominant (COCH gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of nonsyndromic neurosensorial deafness (GJB2 and GJB6 genes)
    • Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2 gene)
    • A.O. S. Andrea
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (entire coding sequence of GJB3, GJB2, GJB6, WFS1, COCH, COL11A2 and MYH9 genes; COCH gene / mutation P51S)
    • Laboratorio de Genética Clínica, S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of nonsyndromic hearing loss and deafness (GJB6 and GJB2 genes)
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (WFS1 gene)
    • A.O.U. Policlinico "G. Martino"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SICILIA
    • MESSINA
    • Molecular diagnosis of Nonsyndromic Sensorineural Deafness (GJB2 gene)
    • AZM - Academisch Ziekenhuis Maastricht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Molecular diagnosis of nonsyndromic sensorineural deafness, types DFNA and DFNB (GJB2, GJB6 genes)
    • Hospital Universitario y Politécnico La Fe
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Preimplantation genetic diagnosis of nonsyndromic sensorineural deafness (GJB2, GJB6, MIR96 genes)
    • Igenomix Spain
    • Purpose(s) : Pre-implantation diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal sensorineural deafness (GJB2 gene)
    • Vilnius University Hospital Santariskiu Klinikos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • LITHUANIA
    • DZUKIJA
    • VILNIUS
    • Autosomal dominant sensorineural deafness type DFNA (gene GJB2 - direct sequencing of exons 1 and 2)
    • Slovak Academy of Sciences
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of non syndromic genetic deafness type DFNB1 (sequencing/MLPA GJB2 and GJB6 genes)
    • Children's University Hospital Zagreb
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CROATIA
    • CROATIA
    • ZAGREB