Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia

Bibliographic Details
Main Authors: Steensma, D, Gibbons, R, Mesa, R, Tefferi, A, Higgs, D
Format: Conference item
Published: 2004

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