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High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

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Manylion Llyfryddiaeth
Prif Awduron: Boultwood, J, Perry, J, Zaman, R, Fernandez-Santamaria, C, Littlewood, T, Kusec, R, Pellagatti, A, Wang, L, Clark, R, Wainscoat, J
Fformat: Journal article
Cyhoeddwyd: 2010
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Eitemau Tebyg

  • High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (2010)
  • Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
    gan: Fernandez-Mercado, M, et al.
    Cyhoeddwyd: (2010)
  • Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (2010)
  • Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (2009)
  • The current knowledge on ASXL1-mutated acute myeloid leukemia
    gan: Marta Andrzejewska, et al.
    Cyhoeddwyd: (2022-02-01)

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