Publicaciones en colaboración con investigadores/as de Klinikum der Universität München (2)

2012

  1. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

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

2009

  1. Clinical predictors for germline mutations in Head and neck paraganglioma patients: cost reduction strategy in Genetic diagnostic process as fail-out

    Cancer Research, Vol. 69, Núm. 8, pp. 3650-3656