Publications in collaboration with researchers from Instituto de Biología y Genética Molecular (4)

2016

  1. Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation

    CASE REPORTS IN NEUROLOGICAL MEDICINE, Vol. 2016

  2. Relevancia de las nuevas pruebas genéticas en el diagnóstico de la talla baja con dismorfias

    Medicina Clinica

2015

  1. Importance of genetic tests in childhood hearing loss

    REVISTA DE LA SOCIEDAD OTORRINOLARINGOLOGICA DE CASTILLA Y LEON CANTABRIA Y LA RIOJA, Vol. 6, pp. 19-30

2007

  1. Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry

    Annals of Human Genetics, Vol. 71, Núm. 2, pp. 194-201