2 Einträge gefunden

1. Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies

   1. Kakar, Naseebullah
   2. Horn, Denise
   3. Decker, Eva
   4. Sowada, Nadine
   5. Kubisch, Christian
   6. Ahmad, Jamil
   7. Borck, Guntram

   2018 - Forschungsinformationssystem des UKE
2. Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation

   1. Danyel, Magdalena
   2. Kortüm, Fanny
   3. Dathe, Katarina
   4. Kutsche, Kerstin
   5. Horn, Denise

   2018 - Forschungsinformationssystem des UKE