Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia.

Παρόμοια τεκμήρια

• Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia
  ανά: Pellagatti, A, κ.ά.
  Έκδοση: (2014)
• Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
  ανά: Fernandez-Mercado, M, κ.ά.
  Έκδοση: (2010)
• Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes.
  ανά: Fernandez-Mercado, M, κ.ά.
  Έκδοση: (2013)
• Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
  ανά: Boultwood, J, κ.ά.
  Έκδοση: (2010)
• Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
  ανά: Fernandez-Mercado, M, κ.ά.
  Έκδοση: (2013)