Näytetään 1 - 2 yhteensä 2 tuloksesta, hakuaika: 0,04s Tarkenna hakua
  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. Tekijä Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

    Julkaistu 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 Tekijä Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

    Julkaistu 2013
    Journal article

Työkalut: