Publications en collaboration avec des chercheurs de Centro Nacional de Investigaciones Oncológicas (3)

2011

  1. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

    Nature Genetics

2007

  1. Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma

    Cancer Research, Vol. 67, Núm. 19, pp. 9561-9567

2004

  1. Genetic and epigenetic profile of sporadic pheochromocytomas.

    Journal of medical genetics, Vol. 41, Núm. 3