2 Einträge gefunden

1. Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder

   1. Harms, Frederike L
   2. Kloth, Katja
   3. Bley, Annette
   4. Denecke, Jonas
   5. Santer, René
   6. Lessel, Davor
   7. Hempel, Maja

   2018 - Forschungsinformationssystem des UKE
2. Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients

   1. Girisha, Katta Mohan
   2. Bidchol, Abdul Mueed
   3. Graul-Neumann, Luitgard
   4. Gupta, Ashish
   5. Hehr, Ute
   6. Lessel, Davor
   7. Nader, Sean

   2016 - Forschungsinformationssystem des UKE - frei zugänglich