6 Einträge gefunden

1. Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.

   1. Schneppenheim, Reinhard
   2. Frühwald, Michael C
   3. Gesk, Stefan
   4. Hasselblatt, Martin
   5. Jeibmann, Astrid
   6. Kordes, Uwe
   7. Kreuz, Markus

   2010 - Forschungsinformationssystem des UKE
2. The problem of novel FVIII missense mutations for haemophilia A genetic counseling.

   1. Schneppenheim, Reinhard
   2. Schröder, J
   3. Obser, Tobias
   4. Oyen, Florian
   5. Schneppenheim, S
   6. Oldenburg, J

   2009 - Forschungsinformationssystem des UKE
3. Response to DDAVP in children with von Willebrand disease type 2.

   1. Schneppenheim, Reinhard
   2. Budde, U
   3. Beutel, Karin
   4. Hassenpflug, W-A
   5. Hauch, H
   6. Obser, Tobias
   7. Oyen, Florian

   2009 - Forschungsinformationssystem des UKE
4. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.

   1. Gupta, P K
   2. Saxena, R
   3. Adamtziki, E
   4. Budde, U
   5. Oyen, Florian
   6. Obser, Tobias
   7. Schneppenheim, Reinhard

   2008 - Forschungsinformationssystem des UKE
5. An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.

   1. Mohl, A
   2. Marschalek, R
   3. Masszi, T
   4. Nagy, E
   5. Obser, Tobias
   6. Oyen, Florian
   7. Sallai, K

   2008 - Forschungsinformationssystem des UKE
6. Gene conversions are a common cause of von Willebrand disease.

   1. Gupta, P K
   2. Adamtziki, E
   3. Budde, U
   4. Jaiprakash, M
   5. Kumar, H
   6. Harbeck-Seu, A
   7. Kannan, M

   2005 - Forschungsinformationssystem des UKE