CAMT in a female with developmental delay, facial malformations and central nervous system anomalies.

dc.contributor.author	Loidi Fernández, Lourdes
dc.contributor.author	Martinon Torres, Nazareth
dc.contributor.author	Couselo Sánchez, José Miguel
dc.contributor.author	Vázquez Donsión, Manuel
dc.date.accessioned	2017-06-07T07:10:32Z
dc.date.available	2017-06-07T07:10:32Z
dc.date.issued	2011
dc.identifier.issn	1545-5009
dc.identifier.uri	http://hdl.handle.net/20.500.11940/3456
dc.language.iso	eng
dc.title	CAMT in a female with developmental delay, facial malformations and central nervous system anomalies.
dc.type	Artigo	es
dc.authorsophos	Martinón-Torres, Nazareth
dc.authorsophos	Vázquez-Donsión, Manuel
dc.authorsophos	Loidi, Lourdes
dc.authorsophos	Couselo, Jose Miguel
dc.identifier.doi	10.1002/pbc.22904
dc.identifier.isi	287006700021
dc.identifier.pmid	21225925
dc.identifier.sophos	9835
dc.issue.number	3
dc.journal.title	PEDIATRIC BLOOD & CANCER
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	452
dc.page.final	453
dc.rights.accessRights	openAccess
dc.typesophos	Artículo Original
dc.volume.number	56

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