A Xq21.31 duplication without features of Prader-Willi syndrome

dc.contributor.author	Barros Angueira, Francisco
dc.contributor.author	Castro Gago, Manuel
dc.contributor.author	Gómez Lado, María del Carmen
dc.contributor.author	Perez Gay, Laura
dc.date.accessioned	2017-06-07T07:10:33Z
dc.date.available	2017-06-07T07:10:33Z
dc.date.issued	2013
dc.identifier.issn	1355-008X
dc.identifier.uri	http://hdl.handle.net/20.500.11940/3461
dc.language.iso	eng
dc.title	A Xq21.31 duplication without features of Prader-Willi syndrome
dc.type	Artigo	es
dc.authorsophos	Castro-Gago, M.
dc.authorsophos	Pérez-Gay, L.
dc.authorsophos	Gómez-Lado, C.
dc.authorsophos	Barros-Angueira, F.
dc.identifier.doi	10.1007/s12020-012-9738-4
dc.identifier.isi	313069600037
dc.identifier.pmid	22763470
dc.identifier.sophos	13194
dc.issue.number	1
dc.journal.title	ENDOCRINE
dc.organization	Consellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.page.initial	238
dc.rights.accessRights	openAccess
dc.typesophos	Artículo de Opinión
dc.volume.number	43

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