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

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

Xehetasun bibliografikoak
Egile Nagusiak: Fernandez-Mercado, M, Pellagatti, A, Perry, J, Fernandez-Santamaria, C, Calasanz, M, Larrayoz, M, Odero, MD, Killick, S, Wainscoat, J, Boultwood, J
Formatua: Conference item
Argitaratua: 2010
  • Aleari buruzko argibideak
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Antzeko izenburuak

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

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