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dc.contributor.authorCarracedo Álvarez, Ángel
dc.contributor.authorGómez Guerrero, Lorena María
dc.contributor.authorFernández Prieto, Montserrat
dc.date.accessioned2017-06-07T07:25:10Z
dc.date.available2017-06-07T07:25:10Z
dc.date.issued2015
dc.identifier.issn1552-4825
dc.identifier.urihttp://hdl.handle.net/20.500.11940/6208
dc.language.isoeng
dc.titleFemale patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion
dc.typeArtigoes
dc.authorsophosQuintela, Ines
dc.authorsophosGomez-Guerrero, Lorena
dc.authorsophosFernandez-Prieto, Montse
dc.authorsophosResches, Mariela
dc.authorsophosBarros, Francisco
dc.authorsophosCarracedo, Angel
dc.identifier.doi10.1002/ajmg.a.37292
dc.identifier.pmid26332054
dc.identifier.sophos20007
dc.issue.number12
dc.journal.titleAMERICAN JOURNAL OF MEDICAL GENETICS PART A
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.page.initial3121
dc.page.final3129
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number167A


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