NCT02804373
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +13 more
- Locations
-
- Centre de référence Prader-Willi - Hôpital Purpan Toulouse, France
Clinical trial condition
Explore clinical trials studying Imprinting Disorders. Study availability and eligibility vary by location and protocol.
NCT02804373
NCT05249998
NCT04428281
NCT02996305
NCT03031626
NCT05153434
NCT06295315
NCT06900335
NCT06851351