Ana Catalan Lamban-rekin lankidetzan egindako argitalpenak (3)

2021

  1. Additional causal SNRPE mutations in hereditary hypotrichosis simplex

    British Journal of Dermatology

  2. Clinical value of NGS genomic studies for clinical management of pediatric and young adult bone sarcomas

    Cancers, Vol. 13, Núm. 21

2020

  1. Somatic and germline analysis of a familial Rothmund–Thomson syndrome in two siblings with osteosarcoma

    npj Genomic Medicine, Vol. 5, Núm. 1