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Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

dc.contributor.authorCarracedo Álvarez, Ángel
dc.contributor.authorBarros Angueira, Francisco
dc.contributor.authorCastro Gago, Manuel 
dc.contributor.authorPerez Gay, Laura 
dc.contributor.authorEiris Puñal, Jesús
dc.contributor.authorDacruz Álvarez, David 
dc.contributor.authorQuintela García, Inés
dc.date.accessioned2017-06-07T06:53:27Z
dc.date.available2017-06-07T06:53:27Z
dc.date.issued2015
dc.identifier.issn0210-0010
dc.identifier.urihttp://hdl.handle.net/20.500.11940/266
dc.language.isoeng
dc.titleMolecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes
dc.typeArtigoes
dc.authorsophosQuintela, I.
dc.authorsophosBarros-Angueira, F.
dc.authorsophosPerez-Gay, L.
dc.authorsophosDacruz, D.
dc.authorsophosCastro-Gago, M.
dc.authorsophosCarracedo, A.
dc.authorsophosEiris-Punal, J.
dc.identifier.isi362274000003
dc.identifier.pmid26350776
dc.identifier.sophos18688
dc.issue.number6
dc.journal.titleREVISTA DE NEUROLOGIA
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Neuroloxía
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.page.initial255
dc.page.final60
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number61


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