4 Einträge gefunden

1. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry

   1. Saha, Bidisha
   2. Lessel, Davor
   3. Nampoothiri, Sheela
   4. Rao, Anuradha S
   5. Hisama, Fuki M
   6. Peter, Dincy
   7. Bennett, Chris

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
2. Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics

   1. Wildhardt, Gabriele
   2. Zirn, Birgit
   3. Graul-Neumann, Luitgard M
   4. Wechtenbruch, Juliane
   5. Suckfüll, Markus
   6. Buske, Annegret
   7. Bohring, Axel

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
3. A rare missense variant abrogates the signaling activity of tetherin/BST-2 without affecting its effect on virus release

   1. Sauter, Daniel
   2. Hotter, Dominik
   3. Engelhart, Susanne
   4. Giehler, Fabian
   5. Kieser, Arnd
   6. Kubisch, Christian
   7. Kirchhoff, Frank

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
4. Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation

   1. Kakar, Naseebullah
   2. Ahmad, Jamil
   3. Kubisch, Christian
   4. Borck, Guntram

   2013 - Forschungsinformationssystem des UKE