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. HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?

   1. Rau, Isabella
   2. Shaw, Gary M
   3. Kutsche, Kerstin

   2007 - Forschungsinformationssystem des UKE