Didascalia
: Accreditato
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- GERMANIA
- 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
- Ulteriori informazioni
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- PAESI BASSI
- 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
- Ulteriori informazioni
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- FRANCIA
- ILE-DE-FRANCE
- PARIS
- Molecular diagnosis of Baraitser-Winter syndrome (ACTB and ACTG1 genes)
- CHU Paris - Hôpital Robert Debré
- Ulteriori informazioni
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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
- Ulteriori informazioni
