Publicaciones en colaboración con investigadores/as de Erasmus University Medical Center (3)

2015

  1. Inventory of current EU paediatric vision and hearing screening programmes

    Journal of Medical Screening, Vol. 22, Núm. 2, pp. 55-64

2012

  1. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

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