Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
Үндсэн зохиолчид: | Steensma, D, Gibbons, R, Mesa, R, Tefferi, A, Higgs, D |
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Формат: | Conference item |
Хэвлэсэн: |
2004
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Ижил төстэй зүйлс
Ижил төстэй зүйлс
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Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.
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RUNX1::CBFA2T2 rearranged acute myeloid leukemia transformed from JAK2 V617F mutated primary myelofibrosis
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DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
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Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
-н: Steensma, D, зэрэг
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Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies.
-н: Steensma, D, зэрэг
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