2 Einträge gefunden

1. More evidence on TRIO missense mutations in the spectrin repeat domain causing severe developmental delay and recognizable facial dysmorphism with macrocephaly

   1. Kloth, K
   2. Graul-Neumann, L
   3. Hermann, K
   4. Johannsen, J
   5. Bierhals, T
   6. Kortüm, F

   2021 - Forschungsinformationssystem des UKE
2. Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination

   1. Chelban, V
   2. Alsagob, M
   3. Kloth, K
   4. Chirita-Emandi, A
   5. Vandrovcova, J
   6. Maroofian, R
   7. Davagnanam, I

   2020 - Forschungsinformationssystem des UKE