Publications in collaboration with researchers from Hospital Universitario La Fe (2)

2015

  1. De novo mutations in PLXND1 and REV3L cause Möbius syndrome

    Nature Communications, Vol. 6

2011

  1. In silico identification of new candidate genes for hereditary congenital facial paresis

    International Journal of Developmental Neuroscience, Vol. 29, Núm. 4, pp. 451-460