Publicaciones en las que colabora con GUIOMAR PEREZ DE NANCLARES LEAL (4)

2008

  1. Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

    Clinical Endocrinology, Vol. 68, Núm. 6, pp. 873-878

2007

  1. Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

    Clinical Endocrinology, Vol. 67, Núm. 4, pp. 538-546

  2. The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities

    Diabetic Medicine, Vol. 24, Núm. 7, pp. 707-713

1996

  1. A case of Prader-Willi syndrome associated with mosaicism: Cytogenetic and FISH study

    Genes and Genetic Systems, Vol. 71, Núm. 1, pp. 31-36