Hospital Clinico Universitario de Valencia -ko ikertzaileekin lankidetzan egindako argitalpenak (3)

2019

  1. DNA Methylation of tumor suppressor genes in pituitary neuroendocrine tumors

    Journal of Clinical Endocrinology and Metabolism, Vol. 104, Núm. 4, pp. 1272-1282

  2. Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: Diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)

    Hereditary Cancer in Clinical Practice, Vol. 17, Núm. 1

2014

  1. Prevalence of germline MUTYH mutations among Lynch-like syndrome patients

    European Journal of Cancer, Vol. 50, Núm. 13, pp. 2241-2250