2 Einträge gefunden

1. Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both c.35delG of GJB2 and the 342-kb deletion involving GJB6.

   1. Bolz, Hanno
   2. Götz, Schade
   3. Ehmer, Stefanie
   4. Kothe, Christian
   5. Hess, Markus
   6. Gal, Andreas

   2004 - Forschungsinformationssystem des UKE
2. Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11).

   1. Bolz, Hanno
   2. Bolz, Steffen-Sebastian
   3. Götz, Schade
   4. Kothe, Christian
   5. Mohrmann, Gerrit
   6. Hess, Markus
   7. Gal, Andreas

   2004 - Forschungsinformationssystem des UKE