Publications in collaboration with researchers from Hospital Vall d'Hebron (2)

2014

  1. Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

    Clinica Chimica Acta, Vol. 437, pp. 88-92

2010

  1. Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

    Molecular Psychiatry, Vol. 15, Núm. 10, pp. 1023-1033