Publicaciones en colaboración con investigadores/as de University of Oxford (3)

2016

  1. Targeted resequencing analysis of 31 genes commonly mutated in myeloid disorders in serial samples from myelodysplastic syndrome patients showing disease progression

    Leukemia

2014

  1. Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia

    Leukemia

2013

  1. Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression

    British Journal of Haematology, Vol. 163, Núm. 2, pp. 235-239