GUSTAVO
PÉREZ DE NANCLARES LEAL
Hospital Universitario Central de Asturias
Oviedo, EspañaHospital Universitario Central de Asturias -ko ikertzaileekin lankidetzan egindako argitalpenak (2)
2015
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Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: Atypical findings and a novel mutation in NR0B1
Journal of Pediatric Endocrinology and Metabolism, Vol. 28, Núm. 9-10, pp. 1129-1137
2012
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Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus
Journal of Clinical Endocrinology and Metabolism, Vol. 97, Núm. 6