प्रदर्शित 1 - 2 परिणाम 2, सवाल का समय: 0.06सेकंड परिणाम को परिष्कृत करें
  1. 1
    Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.

    Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. द्वारा Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

    प्रकाशित 2013
    Journal article
  2. 2
    Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression

    Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression द्वारा Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

    प्रकाशित 2013
    Journal article

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