4 Einträge gefunden

1. A novel 9 bp deletion in the filamin a gene causes an otopalatodigital-spectrum disorder with a variable, intermediate phenotype.

   1. Stefanova, Margarita
   2. Meinecke, Peter
   3. Gal, Andreas
   4. Bolz, Hanno

   2005 - Forschungsinformationssystem des UKE
2. Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies.

   1. Bolz, Hanno
   2. Ebermann, Inga
   3. Gal, Andreas

   2005 - Forschungsinformationssystem des UKE - frei zugänglich
3. 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
4. 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