Publicaciones en colaboración con investigadores/as de Hospital de Fuenlabrada (3)

2022

  1. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients

    Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1

2015

  1. Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene

    Journal of the National Cancer Institute, Vol. 107, Núm. 5

2013

  1. Influence of RET mutations on the expression of tyrosine kinases in medullary thyroid carcinoma

    Endocrine-Related Cancer, Vol. 20, Núm. 4, pp. 611-619