Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/78852
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dc.contributor.authorJolley, A.en
dc.contributor.authorCorbett, M.en
dc.contributor.authorMcGregor, L.en
dc.contributor.authorWaters, W.en
dc.contributor.authorBrown, S.en
dc.contributor.authorNicholl, J.en
dc.contributor.authorYu, S.en
dc.date.issued2013en
dc.identifier.citationAmerican Journal of Medical Genetics. Part A, 2013; 161(6):1508-1512en
dc.identifier.issn1552-4825en
dc.identifier.issn1552-4833en
dc.identifier.urihttp://hdl.handle.net/2440/78852-
dc.description.statementofresponsibilityAlexandra Jolley, Mark Corbett, Lesley McGregor, Wendy Waters, Susan Brown, Jillian Nicholl, and Sui Yuen
dc.language.isoenen
dc.publisherWiley-Lissen
dc.rightsCopyright © 2013 Wiley Periodicals, Inc.en
dc.subjectHumans; Chromosome Deletion; Translocation, Genetic; Proteins; Cytoskeletal Proteins; Transcription Factors; In Situ Hybridization, Fluorescence; Autistic Disorder; Developmental Disabilities; Base Sequence; Adolescent; Male; Comparative Genomic Hybridization; Chromosome Inversionen
dc.titleDe novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature reviewen
dc.typeJournal articleen
dc.identifier.rmid0020128894en
dc.identifier.doi10.1002/ajmg.a.35922en
dc.identifier.pubid19187-
pubs.library.collectionObstetrics and Gynaecology publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidCorbett, M. [0000-0001-9298-3072]en
Appears in Collections:Obstetrics and Gynaecology publications

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