Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
Hlavní autoři: | Steensma, D, Gibbons, R, Mesa, R, Tefferi, A, Higgs, D |
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Médium: | Conference item |
Vydáno: |
2004
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