Publications by the researcher in collaboration with Francisco Barros Angueira (3)

2018

  1. V232D mutation in patients with cystic fibrosis Not so rare, not so mild

    Medicine (United States), Vol. 97, Núm. 28

2014

  1. A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

    Journal of Medical Genetics, Vol. 51, Núm. 7, pp. 475-478

  2. Progressive heterotopic ossification: The arduousness of an accurate diagnosis

    Journal of Pediatrics, Vol. 164, Núm. 1, pp. 203-204