3 Einträge gefunden

1. A novel FAM20C mutation causing hypophosphatemic osteomalacia with osteosclerosis (mild Raine syndrome) in an elderly man with spontaneous osteonecrosis of the knee

   1. Rolvien, T
   2. Kornak, U
   3. Schinke, T
   4. Amling, M
   5. Oheim, R

   2019 - Forschungsinformationssystem des UKE
2. Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2

   1. Butscheidt, S
   2. Delsmann, A
   3. Rolvien, T
   4. Barvencik, F
   5. Al-Bughaili, M
   6. Mundlos, S
   7. Schinke, T

   2018 - Forschungsinformationssystem des UKE
3. A novel COL1A2 C-propeptide cleavage site mutation causing high bone mass osteogenesis imperfecta with a regional distribution pattern

   1. Rolvien, T
   2. Kornak, U
   3. Stürznickel, J
   4. Schinke, T
   5. Amling, M
   6. Mundlos, S
   7. Oheim, R

   2018 - Forschungsinformationssystem des UKE