Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia

Παρόμοια τεκμήρια

• Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
  ανά: Boultwood, J, κ.ά.
  Έκδοση: (2010)
• Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
  ανά: Boultwood, J, κ.ά.
  Έκδοση: (2009)
• Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia
  ανά: Pellagatti, A, κ.ά.
  Έκδοση: (2014)
• Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia.
  ανά: Pellagatti, A, κ.ά.
  Έκδοση: (2014)
• High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
  ανά: Boultwood, J, κ.ά.
  Έκδοση: (2010)