INVESTIGACIÓN EN ENFERMEDADES RARAS
Hospital General Universitario Reina Sofía
Murcia, EspañaPublicaciones en colaboración con investigadores/as de Hospital General Universitario Reina Sofía (2)
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
2010
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New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism
European Journal of Endocrinology, Vol. 163, Núm. 6, pp. 953-962