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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • SAINT-OUEN-L'AUMÔNE
    • Accreditation
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 and GJB6 genes)
    • Laboratoire Cerba
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • SAINT-OUEN-L'AUMÔNE
    • Accreditation
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (mutations MT-RNR1: A 1555G, MT-TS1: A 7445C)
    • Laboratoire Cerba
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis recessive nonsyndromic sensorineural deafness DFNB (GJB2, GJB6, SLC26A4 genes)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular diagnosis of nonsyndromic deafness DNFB type (GJB2 and OTOF gene mutations; GJB6 gene deletions)
    • CHU de Marseille - Hôpital de la Timone
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular diagnosis of X-linked nonsyndromic sensorineural deafness type DFN (PRPS1 gene)
    • CHU de Marseille - Hôpital de la Timone
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICĘTRE
    • Accreditation
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • GHU Paris-Sud - Hôpital de Bicętre
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENČVE
    • Accreditation
    • Molecular diagnosis of deafness nonsyndromic (GJB2, GJB6 genes)
    • Centre Médical Universitaire - CMU
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Accreditation
    • Molecular diagnosis of isolated deafness (CX26, CX30, OTOF genes)
    • Azienda Ospedaliero Universitaria Careggi
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Charité - Universitätsmedizin Berlin (CVK)
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Ruhr-Universität Bochum
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinische Hochschule Hannover
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular diagnosis of Gusher syndrome (POU3F4 gene)
    • Medizinische Hochschule Hannover
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Labor Lademannbogen
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3 and GJB6 genes)
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of aminoglycoside-induced deafness (MTRNR1 gene)
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes: sequencing)
    • Pränatalmedizin München
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÖNCHENGLADBACH
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Medizinische Versorgungszentrum Dr.Stein + Kollegen
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÖNCHENGLADBACH
    • Accreditation
    • Molecular diagnosis of aminoglycoside-induced deafness (MTRNR1 gene)
    • Medizinische Versorgungszentrum Dr.Stein + Kollegen
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Paxis und Labor Dr. med Karl Mehnert
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsklinikum Ulm
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (WFS1 gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of X-linked non syndromic sensorineural deafness type DFN (PRPS1 gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness (GJB2 and GJB6 genes)
    • Genetica AG
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of autosomal recessive non syndromic sensorineural deafness (CDH23, CLDN14, DFNB31, DFNB59, ESPN, ESRRB, GJB2, GJB6, HGF, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, PCDH15, RDX, SLC26A4, SLC26A4, STRC, TECTA, TMC1, TMIE, TMPRSS3, TRIOBP, USH1C genes: sequencing, linkage analysis)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of autosomal dominant non syndromic sensorineural deafness (ACTG1, CCDC50, COCH, COL11A2, 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
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of mitochondrial deafness (MTRNR1, MTTS1 genes)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of Gusher syndrome (POU3F4 gene)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of Recessive congenital deafness (GJB2 gene (30delG))
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of Autosomal dominant nonsyndromic sensorineural deafness, DFNA9 (COCH gene (P51S))
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Accreditation
    • Molecular diagnosis of recessive nonsyndromic sensorineural deafness DFNB1 (GJB2 & GJB6 genes)
    • Ghent University Hospital - UZGent
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Accreditation
    • Molecular diagnosis recessive nonsyndromic sensorineural deafness (GJB2 and GJB6 genes)
    • CHU de LIEGE - UniLab Lg
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Nonsyndromic Hearing Loss and Deafness due to connexin 26 anomaly (GJB2 gene)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of autosomal dominant nonsyndromic genetic deafness (WFS1 and COCH genes)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of autosomal recessive nonsyndromic genetic deafness (GJB2, GJB6 and SLC26A4 genes)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of deafness due to connexin 26 anomaly
    • Erasme Hospital - ULB
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of deafness, sensorineural, type 1 (Connexin 26 and 30)
    • Erasme Hospital - ULB
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 and GJB6 genes)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2 and GJB6 genes)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes: sequencing / MLPA)
    • Universität Würzburg - Biozentrum
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of autosomal recessive non syndromic sensorineural deafness (OTOF gene)
    • Universität Würzburg - Biozentrum
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 gene)
    • Birmingham Women's NHS Foundation Trust
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of aminoglycoside-induced deafness (MTRNR1 gene: sequencing, MLPA)
    • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Autosomal Recessive Neurosensory Deafness (DFNB1, GJB2 and GJB6 genes; mitochondrial m.1555A>G analysis)
    • University Hospital of Wales
    • More information
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Accreditation
    • Molecular diagnosis of Non-syndromic Deafness (GJB2 & GJB6 genes)
    • Ninewells Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of deafness due to Connexin 26 anomaly (GJB2 gene)
    • Great Ormond Street Hospital NHS Trust
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Aminoglycoside-induced Deafness (MTRNR1 gene)
    • Great Ormond Street Hospital NHS Trust
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Gusher syndrome - X-linked Deafness (POU3F4 gene)
    • Great Ormond Street Hospital NHS Trust
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB6 and SLC26A4 genes: sequencing / MLPA)
    • GenteQ GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Zentrum für Humangenetik Mannheim
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Nonsyndromic genetic deafness (GJB2 and GJB6 genes)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Mitochondrial nonsyndromic sensorineural deafness (MT-TL1 gene: m.3243A>G, MT-RNR1 gene: m.1555A>G and by whole mitochondria genome sequencing)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • 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
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Autosomal Recessive Deafness (GJB2, GJB6, MYO15A, TMPRSS3, OTOF, TECTA, MYO6, DFNB59, LOXHD1 and TPRN gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of X-linked Deafness (POU3F4 and SMPX gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Deafness (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and SLC26A4 genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of X-linked non syndromic sensorineural deafness type DFN (PRPS1 gene)
    • Praxis für Humangenetik Freiburg
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular diagnosis of Autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 (Cx26) and GJB6 (Cx30) genes)
    • Southmead Hospital
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (m.1555A>G in MTRNR1 gene)
    • Birmingham Children's Hospital
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • 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.
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • 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.
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • 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
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of autosomal recessive non syndromic sensorineural deafness (CIB2, GJB2, GJB3, GJB6, HGF, MYO15A, MYO3A, MYO7A, OTOF, PCDH15, SLC26A4, STRC, TMC1, TMIE , TRIOBP, USH1C genes)
    • Centogene AG
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Accreditation
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene: 35delG mutation)
    • United Medix Laboratories Ltd.
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB1, GJB2, GJB3, GJB4 and GJB6 genes)
    • Zentrum für Humangenetik
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Accreditation
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness, dominant or recessive (GJB2 gene)
    • Complejo Asistencial Universitario de Salamanca
    • More information
    • SWEDEN
    • Västra Götalandsregionen
    • GÖTEBORG
    • Accreditation
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 gene)
    • Sahlgrenska University Hospital
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BERN
    • Accreditation
    • Molecular diagnosis of non syndromic hearing loss and deafness DFNA9 (COCH gene)
    • Inselspital
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BERN
    • Accreditation
    • Molecular diagnosis of nonsyndromic hearing loss and deafness DFNB1 (GJB2 and GJB6 genes)
    • Inselspital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Preimplantation molecular diagnosis of Autosomal recessive nonsyndromic sensorineural deafness type 1A - DFNB1A (GJB2: by linkage and mutation analysis)
    • Institute for Women's Health
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Accreditation
    • Molecular diagnosis of DFNB1-caused Non-Syndromic Genetic Deafness (full GJB2 coding region sequencing, exon 1 splice site mutation analysis and GJB6 deletion analysis)
    • St James's University Hospital
    • More information
    • GERMANY
    • Baden-Württemberg
    • SINGEN /HTWL.
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für Laboratoriumsmedizin und Humangenetik
    • More information
    • GERMANY
    • Baden-Württemberg
    • SINGEN /HTWL.
    • Accreditation
    • Molecular diagnosis of Gusher syndrome (POU3F4 gene)
    • Institut für Laboratoriumsmedizin und Humangenetik
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Accreditation
    • Preimplantation genetic diagnosis of autosomal recessive nonsyndromic sensorineural deafness (GJB2 gene)
    • Sistemas Genómicos S.L.
    • More information
    • CZECH REPUBLIC
    • Plzen
    • PLZEN
    • Accreditation
    • Molecular diagnosis of non syndromic genetic deafness type DFNB1 (GJB2 and GJB6 genes)
    • Genetika Plzen
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of autosomal dominant sensorineural deafness type 6 (WFS1 gene: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of autosomal recessive non syndromic sensorineural deafness type DFNB (CDH23, DFNB31, GJB2, GJB6, KCNJ10, MYO7A, PCDH15 genes: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3, GJB6, MYH9, SLC26A4 genes)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of X-linked non syndromic sensorineural deafness type DFN (PRPS1 gene)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of genetic nonsyndromic deafness: search for mutations of GJB2, GJB3 and GJB6 genes
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Molecular diagnosis of non syndromic genetic deafness (GJB2, GJB6, TECTA, MYO15A, OTOF, TMC1, MT-RNR1 genes)
    • IURC - Institut Universitaire de Recherche Clinique
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of deafness due to connexin 26 and 30 anomalies (coding sequences and promoters of GJB2 and GJB6 genes)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of isolated deafness due to mitochondrial transmission (MT-RNR1, MT-TL1 and MT-TS1 known gene mutations)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • 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
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of recessive non syndromic genetic deafness DFNB (Q829X mutation in OTOF gene)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of X-linked nonsyndromic sensorineural deafness type DFN (PRPS1 gene)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness (GJB2, GJB6, OTOF and COCH genes)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Pharmacogenetic analysis of aminoglycoside ototoxicity (MT-RNR1 and MT-TS1 genes)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (mitochondrial DNA)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular diagnosis of non syndromic deafness (GJB2 gene)
    • CHRU de Brest - Hôpital Morvan
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene)
    • CHRU de Brest - Hôpital Morvan
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • POISSY
    • Molecular diagnosis of non syndromic genetic deafness (GJB2, GJB6, MT-RNR1 genes)
    • Centre hospitalier intercommunal Poissy-Saint-Germain-en-Laye
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Molecular diagnosis of deafness due to connexin 26 and 30 anomaly (GJB2 and GJB6 genes)
    • CHU de Reims - Hôpital Maison Blanche
    • More information
    • FRANCE
    • POITOU-CHARENTES
    • POITIERS
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 gene)
    • CHU de Poitiers
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of genetic deafness
    • Tecnobios Prenatale S.r.L.
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of deafness due to connexin types (GJA1,GJB6,GJB2 genes)
    • Ospedali Galliera
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of isolated deafness due to mitochondral transmission (MTRNR1,MTTS1 genes)
    • Ospedali Galliera
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of conductive deafness with stapes fixation (POU3F4 gene)
    • Ospedali Galliera
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of non syndromic deafness due to connexin 26 anomaly (GJB2, GJB6 genes)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Molecular diagnosis of nonsyndromic sensorineural dafness (GJB2 gene)
    • LABOGEN S.a.S.
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of isolated deafness due to mitochondrial transmission (mithocondrial DNA)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of non syndromic deafness due to connexin anomalies (GJB2, GJB6 genes)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of non syndromic deafness due to connexines 26 and 30 anomaly (GJB2 and GJB6 genes)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of non syndromic mithocondrial deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Istituto CSS-Mendel
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of deafness due to mitochondrial transmission (MTRNR1 gene)
    • Istituto CSS-Mendel
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of connexin 26 and 30 deafness (GJB6-D13S80)
    • Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB6 genes)
    • Biotecnologie Avanzate Srl
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of deafness, isolated, due to mitochondrial transmission (MT-CO1, MT-RNR1 genes)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of nonsyndromic deafness due to connexin anomalies 26, 30 and 31
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of nonsyndromic sensorineural deafness, autosomal dominant (COCH gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • SPAIN
    • Asturias
    • OVIEDO
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene / mutation A1555G)
    • Hospital Universitario Central de Asturias
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2, GJB6 genes)
    • Laboratorio Genoma
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praenatal-Medizin und Genetik, Düsseldorf
    • More information
    • GERMANY
    • Bayern
    • ERLANGEN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsklinikum Erlangen
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes: sequencing)
    • Universitätsklinikum Freiburg
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsmedizin Göttingen
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of connexin 26 anomaly
    • Centro de Análisis Genéticos
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Laborärztlich-humangenetische Partnerschaft Eiben - Glaubitz
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Molecular diagnosis of non-syndromic deafness (GJA1, GJB2, GJB3, GJB6 and MT-RNR1 genes)
    • Ospedale Regionale per le Microcitemie
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für angewandte Humangenetik und Onkogenetik
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 and GJB6 genes)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • SPAIN
    • Canarias
    • LAS PALMAS DE GRAN CANARIA
    • Molecular diagnosis of congenital deafness (GJB2 gene)
    • Complejo Hospitalario Universitario Insular-Materno Infantil
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of non-syndromic deafness (GJB2, GJB6 genes)
    • Azienda Ospedaliera Universitaria di Padova
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of isolated deafness due to mitochondrial transmission (MT-RNR1, MT-TS1 genes)
    • Azienda Ospedaliera Universitaria di Padova
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of nonsyndromic genetic deafness (SLC26A4 gene)
    • Azienda Ospedaliera Universitaria di Padova
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • FERRARA
    • Molecular diagnosis of non syndromic deafness due to connexines 26 and 30 (GJB2, GJB 6 genes)
    • Azienda Ospedaliero-Universitaria di Ferrara
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Molecular diagnosis of autosomal dominant non syndromic genetic deafness (GJB2 and GJB6 genes)
    • CHU de Lyon-GH Est - Hospices Civils de Lyon
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 gene)
    • Hospital Universitario Virgen del Rocío
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsklinikum Köln
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of aminoglycoside-induced deafness (MTRNR1 gene)
    • Universitätsklinikum Köln
    • More information
    • GERMANY
    • Niedersachsen
    • HILDESHEIM
    • Molecular diagnosis of connexin 26 linked nonsyndromic deafness
    • Gemeinschaftspraxis Dres. Algermissen / Justus / Wilke / Graf
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BASEL
    • Molecular diagnosis of recessive nonsyndromic sensorineural deafness DFNB1 (GJB2 and GJB6 genes)
    • Universitätsspital Basel
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Molecular diagnosis of genetic nonsyndromic deafness, due to connexin 26 anomalies (GJB2 gene)
    • CPSS - Centro Polidiagnostico Servizi Sanitari
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of sensorineural deafness (GJB2 gene sequencing)
    • University of Turku
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Congenital deafness (GJB2, GJB3 and GJB6 genes): sequencing of the entire coding region and delection analysis by MLPA
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Congenital deafness, X-linked (POU3F4 gene): Sequencing of entire coding region and delection analysis by MLPA
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Mitochondrial congenital deafness (MTRNR1 and MTTS1 genes): Sequencing of entire coding region for MTRNR1 gene and Sequencing of targeted mutations (7445A>G, 7511T>C, 7510T>C, 7511C>C, 7472insC) for MTTS1 gene
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Non-syndromic congenital deafness (GJB6, SLC26A4, OTOF genes): Sequencing of entire coding region
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of congenital deafness (WFS1 gene): sequencing of the entire coding region and delection analysis by MLPA
    • Instituto de Biologia Molecular e Celular
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of nonsyndromic sensorineural deafness, types DFNA and DFNB (GJB2, GJB6 genes)
    • Hospital Universitario La Fe (Campanar)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-TS1 gene)
    • Hospital Universitario La Fe (Campanar)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • 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.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (OTOF, GJB2, GJB6, MYO7A, MYO15A, SLC26A4, TMC1, CDH23, USH1C, TECTA, MYO3A, MYO6, HGF, PCDH15, COL11A2, TRIOBP, RDX, LOXHD1, PTPRQ, SLC26A5 genes)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene)
    • Sistemas Genómicos S.L.
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinische Universität Graz
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Molecular diagnosis of deafness nonsyndromic sensorineural (GJB2, GJB3, GJB6, GJA1, SLC26A4, and SLC26A5 genes)
    • Tartu University Hospital
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praxis Dres. Gencik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinische Universität Wien
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Klinikum Stuttgart - Standort Olgahospital
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Molecular diagnosis of sensorineural deafness DFNA17 (MYH9 gene)
    • Praxis Dr. Mato Nagel
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness type DFNA and DFNB (GJB2 and GJB6 genes)
    • Faculdade de Medicina da Universidade de Lisboa
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • Molecular diagnosis of Gusher syndrome (POU3F4 gene)
    • CHRU de Tours - Hôpital Bretonneau
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 and GJB6 genes)
    • Fundación Jiménez Díaz
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 and MT-TS1 genes)
    • Fundación Jiménez Díaz
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Praxis für Humangenetik
    • More information
    • HUNGARY
    • Dél-Dunántúl
    • PECS
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • Clinical Center - University of Pécs
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Molecular diagnosis of congenital deafness (GJB2 &GJB6 genes)
    • Université Catholique de Louvain - UCL
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Molecular diagnosis of recessive non syndromic genetic deafness DFNB9 (OTOF gene)
    • Université Catholique de Louvain - UCL
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of connexin 26 and 30 anomalies (GJB2 and GJB6 genes)
    • Diagnostic Genetic Center
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Molecular diagnosis of deafness due to connexin 26 and 30 anomalies (GJB2 and GJB6 genes)
    • The Cyprus Institute of Neurology and Genetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • 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
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of X-linked sensorineural deafness (POU3F4 gene: Analysis of the entire coding region - sequence analysis)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of OTOF-related deafness: sequencing of the entire coding region
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • 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
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of macrothrombocytopenia and progressive sensorineural deafness (MYH9 gene: sequencing of entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Preimplantation genetic diagnosis of the nonsyndromic genetic deafness autosomal recessive. GJB2 gene
    • Reprogenetics Spain S.A.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (OTOF gene / gene and exons 11 ans 12 sequencing; GJB2 gene / entire coding sequence and mut. 35delG; GJB6 gene / entire coding sequence; SLC26A4 gene / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2, GJB6 genes / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of Mitochondrial aminoglycoside induced deafness (MT-TS1 & MT-RNR1 genes)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • Gennet s.r.o.
    • More information
    • NORWAY
    • Nord-Norge
    • TROMSŘ
    • Molecular diagnosis of non syndromic deafness due to connexin 26 anomaly
    • UNN - Universitetssykehuset Nord-Norge - University hospital of North Norway
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene: 35delG, 313del14 and IVS1+1G>A mutations)
    • Institute of mother and child / Instytut Matki i Dziecka
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • Genexpress Ltd.
    • More information
    • HUNGARY
    • Észak-Magyarország
    • BUDAPEST
    • Molecular diagnosis of nonsyndromic genetic deafness by PCR-RFLP (GJB2 gene)
    • Semmelweis University
    • More information
    • SLOVENIA
    • SLOVENIA
    • MARIBOR
    • Molecular diagnosis of nonsyndromic genetic deafness
    • Maribor general hospital
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of sensorineural deafness (GJB2, GJB3 and GJB6 genes)
    • Universitätsklinikum Münster
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of nonsyndromic hereditary deafness due to connexin 26 anomalies
    • Karolinska University Hospital - Solna
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • Genetiks - Genetic diagnosis and research center
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Institut für Klinische Genetik Bonn
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of aminoglycoside-induced deafness (MTRNR1 gene)
    • Institut für Klinische Genetik Bonn
    • More information
    • SLOVENIA
    • SLOVENIA
    • LJUBLJANA
    • Molecular diagnosis of Congenital hearing-loss (GJB2 gene)
    • University Medical Centre Ljubljana
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Deafness non-syndromic (GJB2, GJB6, Mutation analysis, PGD)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • RAMAT-GAN
    • Molecular diagnosis of DFNB1 non-syndromic hearing loss (GJB2, GJB6, Mutation analysis, Carrier detection, PGD)
    • Sheba Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • RAMAT-GAN
    • Molecular diagnosis of Deafness (mitochondrial) (MTRNR1)
    • Sheba Medical Center
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Molecular diagnosis of sensorineural deafness (COCH and GJB2, 3, and 6 genes)
    • Medizinische Universität Innsbruck
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Universitätsmedizin Mainz
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Molecular diagnosis of mitochondrial deafness (MTRNR1 gene)
    • Universitätsmedizin Mainz
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene: mutations 35delG and 313del14)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • DENMARK
    • Syddanmark
    • VEJLE
    • Molecular diagnosis of non syndromic genetic deafness (frequent deletions in GJB2 and GJB6 genes detected by MLPA)
    • Sygehus Lillebaelt Vejle Hospital
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of nonsyndromic genetic deafness (GJB2, GJB6 and OTOF genes)
    • Genetaq
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (DFNB59 gene)
    • Genetaq
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene: mutations: A1555G, C1494T, T1095C)
    • Genetaq
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of sensorineural deafness (GJB6 gene: hotspot)
    • Praxis für Humangenetik und Prävention
    • More information
    • ITALY
    • VENETO
    • NOVENTA VICENTINA
    • Molecular diagnosis of non syndromic deafness due to connexin 26 (CX26 gene)
    • GENETICLAB Srl
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene: 35delG, 310del14 and IVS1+1G>A as well as of the rare mutations in the coding region; frequent mutations in the GJB6 gene)
    • Nzoz Genomed
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 and OTOF genes)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (COCH gene - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of postlingual nonsyndromic genetic deafness (GJB2, GJB6, OTOF and MT-RNR1 genes)
    • Secugen S.L.
    • More information
    • GERMANY
    • Bremen
    • BREMEN
    • Molecular diagnosis of sensorineural deafness (GJB2 gene)
    • Praxis für Humangenetik
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • MVZ Humangenetik Ulm
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness (GJB2 gene)
    • IRCCS Ospedale Pediatrico Bambino Gesů
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of sensorineural deafness (GJB2 gene: sequencing / MLPA; GJB6 gene: MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2, GJB6, OTOF genes)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2, GJB6 genes)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • GREECE
    • GREECE
    • THESSALONIKI
    • Molecular diagnosis of autosomal nonsyndromic sensorineural deafness (GJB2 gene)
    • Eurogenetica SA
    • More information
    • SPAIN
    • Andalucía
    • CÁDIZ
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2 gene)
    • Hospital Puerta del Mar
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene: 35delG, 310del14 and IVS1+1G>A as well as of the rare mutations in the coding region; frequent mutations in the GJB6 gene)
    • MEDGEN
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene)
    • Hospital Universitari General Vall d'Hebron
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • 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
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB6 gene / sequencing)
    • Universidad de Salamanca. Facultad de Medicina
    • More information
    • ITALY
    • SICILIA
    • AVOLA
    • Molecular diagnosis of connexin 26 and 30 deafness (GJB2, GJB6 genes)
    • Laboratori Campisi s.r.l.
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene)
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of nonsyndromic deafness (GJB2, MT-RNR genes)
    • Azienda Ospedaliera S. Camillo-Forlanini
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of connexin 26 deafness (GJB2 gene)
    • A.O. Cittŕ della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of isolated deafness due to mitochondrial transmission
    • A.O. Cittŕ della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • BIOS S.p.A.
    • More information
    • ITALY
    • UMBRIA
    • PERUGIA
    • Molecular diagnosis of nonsyndromic deafness due to connexin 26 anomaly
    • Universitŕ degli Studi di Perugia - Ospedale S. Maria della Misericordia
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of mithocondrial sensorineural deafness (mtDNA: MTCO1, MTRNR1, MTTS1genes)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 deafness (GJB2 gene)
    • Centro Medico Artemisia
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • TRIESTE
    • Molecular diagnosis of connexin 26 and 30 deafness (GJB2, GJB6 genes)
    • IRCCS Burlo Garofolo - Istituto per l'Infanzia
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of connexin 26 and 30 anomalies and genetic deafness (GJB2 and GJB6 genes)
    • Ospedale Niguarda Ca' Granda
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular diagnosis of connexines 26 and 30 anomalies
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • More information
    • ITALY
    • BASILICATA
    • MATERA
    • Molecular diagnosis of genetic nonsyndromic deafness (GJB2 and GJB6 genes)
    • Presidio Ospedaliero "Madonna delle Grazie" - Azienda Sanitaria di Matera (ASM)
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexines 26, 30 and 31 anomaly (GJB2, GJB3 and GJB6 genes)
    • Policlinico Universitario "A. Gemelli"
    • More information
    • ITALY
    • LOMBARDIA
    • VARESE
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJA1, GJB2, GJB3, GJB6, MIR96 genes)
    • A.O.U. Ospedale di Circolo e Fondazione Macchi - Universitŕ dell'Insubria
    • More information
    • ITALY
    • LOMBARDIA
    • VARESE
    • Molecular diagnosis of isolated deafness, due to mitochondrial transmission
    • A.O.U. Ospedale di Circolo e Fondazione Macchi - Universitŕ dell'Insubria
    • More information
    • ITALY
    • LOMBARDIA
    • PAVIA
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Fondazione IRCCS Policlinico San Matteo
    • More information
    • ITALY
    • LOMBARDIA
    • BRESCIA
    • Molecular diagnosis of non syndromic deafness due to connexines 26 and 30 (GJB2 and GJB6 genes)
    • Universitŕ degli Studi di Brescia
    • More information
    • ITALY
    • LOMBARDIA
    • BRESCIA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (TFB1M, MT-CO1, MT-RNR1, MT-TH and MT-TS1 genes)
    • Universitŕ degli Studi di Brescia
    • More information
    • GERMANY
    • Bayern
    • NÜRNBERG
    • Molecular diagnosis of sensorineural deafness (GJB2 and GJB6 genes)
    • Medizinisches Versorgungszentrum
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of connexin 26 and 30 anomaly (GJB2 and GJB6 genes)
    • Azienda Ospedaliera di Bologna - Policlinico S. Orsola-Malpighi
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of nonsyndromic mitochondrial sensorineural deafness (MT-RNR1 gene / mutacion 1555A-G)
    • Hospital Universitario Donostia
    • More information
    • ITALY
    • SICILIA
    • TROINA
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • IRCCS OASI Maria Santissima
    • More information
    • ITALY
    • SICILIA
    • MESSINA
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (WFS1 gene)
    • A.O.U. Policlinico "G. Martino"
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of nonsyndromic hearing loss and deafness (GJB6 and GJB2 genes )
    • CGMJM - Centro de Genética Médica Jacinto Magalhăes
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of hereditary nonsyndromic deafness with susceptibility to aminoglycoside exposure. MT-RNR1 gene.
    • Hospital Universitario Ramón y Cajal
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • 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
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of d.eafness, autosomal recessive, nonsyndromic, sensorineural, type DFNB (ESRRB, OTOF, LHFPL5, MYO7A, PCDH15, DFNB59, MARVELD2, GJB2, GJB6, MYO15A, TMIE, TMC1, TMPRSS3, CDH23, USH1C, TECTA, TRIOBP genes)
    • Hospital Universitario Ramón y Cajal
    • More information
    • SPAIN
    • Cantabria
    • SANTANDER
    • Molecular diagnosis of nonsyndromic genetic deafness (GJB2 and GJB6 genes)
    • Instituto de Formación e Investigación Marqués de Valdecilla (IFIMAV)
    • More information
    • SPAIN
    • Cantabria
    • SANTANDER
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene)
    • Instituto de Formación e Investigación Marqués de Valdecilla (IFIMAV)
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2 gene)
    • A.O. S. Andrea
    • More information
    • FINLAND
    • Finland
    • OULU
    • Molecular diagnosis of sensorineural deafness: sequencing of the GJB2 gene
    • Oulu University Hospital
    • More information
    • SPAIN
    • Extremadura
    • MÉRIDA
    • Molecular diagnosis of isolated deafness due to mitochondrial transmission
    • Hospital de Mérida
    • More information
    • SPAIN
    • Extremadura
    • MÉRIDA
    • Molecular diagnosis of deafness due to connexin 26 anomaly
    • Hospital de Mérida
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of deafness, neurosensory (connexin 26 and 30)
    • Allgemeines Krankenhaus
    • More information
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Molecular diagnosis of non syndromic genetic deafness (complete GJB2 gene sequencing)
    • Université Saint-Joseph
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • TRIESTE
    • Molecular diagnosis of genetic nonsyndromic deafness
    • IRCCS Burlo Garofolo - Istituto per l'Infanzia
    • More information
    • ITALY
    • LOMBARDIA
    • BOSISIO PARINI
    • Molecular diagnosis of non syndromic deafness (DNFB1) (GJB2 gene)
    • IRCCS "E. Medea"
    • More information
    • ITALY
    • MARCHE
    • FANO
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Associazione Cante di Montevecchio
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of connexin 26 anomaly (GJB2 gene)
    • Istituto di Diagnostica Clinica Proda
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • USI - Unione Sanitaria Internazionale
    • More information
    • CZECH REPUBLIC
    • South Moravia
    • BRNO
    • Molecular diagnosis of deafness due to connexin 26 anomaly (GJB2 gene)
    • University hospital Brno
    • More information
    • CZECH REPUBLIC
    • Olomouc
    • OLOMOUC
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 gene)
    • University hospital Olomouc
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • LUDWIGSHAFEN
    • Molecular diagnosis of mitochondrial deafness (MTRNR1 gene: 1095C/T, 1555A/G: MTTS1 gene: 7472insC, 7445A/G; MTTQ gene: 4336T/C)
    • Klinikum der Stadt Ludwigshafen gGmbH
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (SLC26A4 gene)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of autosomal recessive non syndromic neurosensory deafness type DFNB1 (GJB2 gene)
    • BURC Genetics Diagnostic Center
    • More information
    • TURKEY
    • TURKEY
    • ANKARA
    • Molecular diagnosis of autosomal recessive non syndromic neurosensory deafness type DFNB1 and DFNB3 (GJB2 gene)
    • Ankara University - Faculty of medicine
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of isolated deafness due to mitochondrial transmission
    • LMU Klinikum der Universität München - Campus Großhadern
    • More information
    • ITALY
    • ABRUZZO
    • CHIETI
    • Molecular diagnosis of neurosensorial deafness (GJB2 gene)
    • Policlinico Universitario di Chieti
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of nonsyndromic neurosensorial deafness (GJB2 and GJB6 genes)
    • Azienda Ospedaliera Universitaria - Seconda Universitŕ degli Studi di Napoli
    • More information
    • ITALY
    • LOMBARDIA
    • MONZA
    • Molecular diagnosis of non syndromic deafness due to connexin 26 anomalies (CX26 gene)
    • Consorzio per la Genetica Molecolare Umana
    • More information
    • BULGARIA
    •  South-West region
    • SOFIA
    • Molecular diagnosis of nonsyndromic hereditary deafness due to connexin 26, 30, 31, 32 and 43 anomalies
    • GENICA
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Deafness non-syndromic (GJB2, GJB6, Mutation analysis)
    • Carmel Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • PETAH TIKVA
    • Molecular diagnosis of Non-syndromic hearing loss (GJB2, GJB6, Mutation analysis)
    • Rabin Medical Center - Beilinson Hospital
    • More information
    • ISRAEL
    • ISRAEL
    • REHOVOT
    • Molecular diagnosis of non-syndromic hearing loss (GJB2, GJB6, Mutation analysis, Carrier detection)
    • Kaplan Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Deafness Non Syndromic (GJB2, GJB6, Mutation analysis, PGD)
    • Shaare Zedek Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular diagnosis of Non-syndromic hearing loss (GJB2, GJB6, Mutation analysis)
    • Wolfson Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular diagnosis of MTTS1-related hearing loss (MT-TS1, sequencing analysis)
    • Wolfson Medical Center
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of aminoglycoside-induced nonsyndromic deafness (MT-RNR1, MT-TS1 and MT-TL1 genes)
    • Institute of Child Health
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene sequencing and detection of common mutations)
    • Institute of Child Health
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Prenatal and postnatal molecular diagnosis of non-syndromic hearing impairement (GJB2 and GJB6 mutation screening)
    • Mitera General, Maternity and Children's Hospital
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (MT-RNR1 gene)
    • The Children's Memorial Health Institute CMHI (IP-CZD)
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of nonsyndromic genetic deafness (GJB2 and GJB6 genes)
    • Warszawski Uniwersytet Medyczny
    • More information
    • LITHUANIA
    • DZUKIJA
    • VILNIUS
    • Molecular diagnosis of autosomal sensorineural deafness (GJB2 gene)
    • Vilnius University Hospital Santariskiu Klinikos
    • More information
    • LITHUANIA
    • DZUKIJA
    • VILNIUS
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness (mutations MT-RNR1: A1555G)
    • Vilnius University Hospital Santariskiu Klinikos
    • More information
    • CZECH REPUBLIC
    • Moravia-Silesia
    • OSTRAVA-PORUBA
    • Molecular diagnosis of non syndromic genetic deafness (GJB2 gene)
    • Laboratory of Forensic Genetics, Laborator forenzni genetiky, spol. s r.o.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of nonsyndromic mitochondrial sensorineural deafness (MT-RNR1 gene / mutations A827G, T961C, T961delT+C(n)ins, T961insC, T961G, T1005C, A1116G, T1291C, T1243C, T1291C, C1494T and A1555G; gene MT-CO1 / mutations T7445C, A7443G, T7472insC and T7511C)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (entire coding sequence of GJB2, GJB6, SLC26A4, OTOF, MC1, MYO15A, TECTA, DFNB59 and TMPRSS3 genes; GJB2 gene / mutation 35delG)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • 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.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Gusher syndrome (entire coding sequence of POU3F4 gene)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of nonsyndromic mitochondrial sensorineural deafness (MT-RNR1 gene / mutations A1555G, A827G, T961C, T961delT+C(n)ins, T961insC, T1005C, A1116G and C1494T; MT-CO1 gene / mutations T7445C and A7443G)
    • Lorgen G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene / mutations A1555G, A827G, T961C, T961delT+C(n)ins, T961insC, T1005C, A1116G and C1494T; MT-CO1 gene / mutations T7445C and A7443G)
    • Lorgen G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (entire coding sequence of GJB2 and GJB6 genes; GJB2 gene / mutation 35delG)
    • Lorgen G.P.
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Molecular diagnosis of Nonsyndromic Sensorineural Deafness (GJB2 gene)
    • AZM - Academisch Ziekenhuis Maastricht
    • More information
    • SPAIN
    • Madrid
    • MAJADAHONDA
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (OTOF and GJB2 genes)
    • Genyca Innova
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (aCGH)
    • Genetadi Biotech S.L.
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene)
    • Hospital Universitario 12 de Octubre
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2, GJB6 genes)
    • ASLRMA - Centro per la tutela della Salute della Donna e del Bambino
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Preimplantation genetic diagnosis of nonsyndromic sensorineural deafness (GJB2, GJB6, MIR96 genes)
    • Iviomics SL
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of autosomal recessive nonsyndromic sensorineural deafness type DFNB (GJB2 gene / sequencing, real time-PCR (p.Gly12Valfs); GJB6 gene / sequencing)
    • GenoClinics
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB2 gene / sequencing, real time-PCR; MYH9, GJB6 genes / sequencing)
    • GenoClinics
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure (MT-RNR1 gene (A1555G) / real-time PCR)
    • GenoClinics
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of Gusher syndrome (POU3F4 gene / sequencing)
    • GenoClinics
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Autosomal dominant sensorineural deafness type DFNA (gene GJB2 - direct sequencing of exons 1 and 2)
    • Slovak Academy of Sciences
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Autosomal recessive nonsyndromic sensorineural deafness type DFNB (gene GJB2 - direct sequencing of exons 1 and 2 and MLPA; gene GJB6 - MLPA analysis)
    • Slovak Academy of Sciences
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ALICANTE
    • Molecular diagnosis of nonsyndromic sensorineural deafness (GJB2 gene / sequencing)
    • Instituto Bernabeu Biotech
    • More information
    • CROATIA
    • CROATIA
    • ZAGREB
    • Molecular diagnosis of non syndromic genetic deafness type DFNB1 (sequencing/MLPA GJB2 and GJB6 genes)
    • Children's University Hospital Zagreb
    • More information