3 Einträge gefunden

1. Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease

   1. Ahmad, F
   2. Oyen, F
   3. Jan, R
   4. Budde, U
   5. Schneppenheim, R
   6. Saxena, R

   2014 - Forschungsinformationssystem des UKE
2. 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
3. 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