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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

Dettagli Bibliografici
Autori principali: Fernandez-Mercado, M, Pellagatti, A, Perry, J, Fernandez-Santamaria, C, Calasanz, M, Larrayoz, M, Odero, MD, Killick, S, Wainscoat, J, Boultwood, J
Natura: Conference item
Pubblicazione: 2010
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Documenti analoghi

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  • High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
    di: Boultwood, J, et al.
    Pubblicazione: (2010)

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