Légende
: Accréditation
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- ALLEMAGNE
- Rheinland-Pfalz
- INGELHEIM AM RHEIN
- 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
- Plus d'informations
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- PAYS-BAS
- Gelderland
- NIJMEGEN
- Molecular diagnosis of Autosomal Dominant Deafness (DIAPH1, KCNQ4, GJB2, GJB6, DFNA5, WFS1, TECTA, COCH, EYA4, MYO7A, COL11A2, POU4F3, MYH9, ACTG1 and MYO6 gene)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Plus d'informations
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Diagnostic moléculaire du syndrome de Baraitser-Winter (gènes ACTB et ACTG1)
- CHU Paris - Hôpital Robert Debré
- Plus d'informations
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- 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
- Plus d'informations
