Publications in collaboration with researchers from Fundación Jiménez Díaz (2)

2020

  1. Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment

    Molecular Vision, Vol. 26, pp. 216-225

2011

  1. Ética en investigación genética (2). Estudios de susceptibilidad

    Medicina Clinica, Vol. 137, Núm. 1, pp. 22-26