2 Einträge gefunden

1. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.

   1. Rau, Isabella
   2. Rauch, Anita
   3. Orth, Ulrike
   4. Schwarzer, Ulrich
   5. Trautmann, Udo
   6. Kutsche, Kerstin

   2007 - Forschungsinformationssystem des UKE
2. Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.

   1. Rau, Isabella
   2. Morleo, Manuela
   3. Rosenberger, Georg
   4. Iaconis, Daniela
   5. Orth, Ulrike
   6. Meinecke, Peter
   7. Lerer, Israela

   2006 - Forschungsinformationssystem des UKE