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

書目詳細資料
Main Authors: Steensma, D, Gibbons, R, Mesa, R, Tefferi, A, Higgs, D
格式: Conference item
出版: 2004

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