Publikationen in Zusammenarbeit mit Forschern von Centro de Investigación Biomédica en Red sobre Enfermedades Raras (2)

2023

  1. Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

    Frontiers in Endocrinology, Vol. 13

2013

  1. Genetics of pheochromocytoma and paraganglioma in Spanish pediatric patients

    Endocrine-Related Cancer