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

Documenti analoghi

• Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.
  di: Steensma, D, et al.
  Pubblicazione: (2005)
• RUNX1::CBFA2T2 rearranged acute myeloid leukemia transformed from JAK2 V617F mutated primary myelofibrosis
  di: Lina Han, et al.
  Pubblicazione: (2024-12-01)
• DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
  di: Steensma, D, et al.
  Pubblicazione: (2003)
• Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
  di: Steensma, D, et al.
  Pubblicazione: (2004)
• Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies.
  di: Steensma, D, et al.
  Pubblicazione: (2005)