Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia

Podobne knjige/članki

• Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
  od: Boultwood, J, et al.
  Izdano: (2010)
• Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
  od: Fernandez-Mercado, M, et al.
  Izdano: (2010)
• Gene Expression Profiling of CD34(+) Cells in Patients with Myelodysplastic Syndromes
  od: Pellagatti, A, et al.
  Izdano: (2008)
• Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
  od: Pellagatti, A, et al.
  Izdano: (2010)
• Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
  od: Pellagatti, A, et al.
  Izdano: (2010)