NCT00899743
- Conditions
- Bone Marrow Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +12 more
- Locations
-
Not specified
Clinical trial condition
Explore clinical trials studying Myeloproliferative Disorders. Study availability and eligibility vary by location and protocol.
NCT00899743
Not specified
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