Publicaciones en colaboración con investigadores/as de Università degli Studi di Brescia (2)

2012

  1. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

    Clinical Cancer Research, Vol. 18, Núm. 10, pp. 2828-2837

2010

  1. Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

    JAMA - Journal of the American Medical Association, Vol. 304, Núm. 23, pp. 2611-2619