1. Adelaide Research & Scholarship
  2. Schools and Disciplines
  3. School of Paediatrics & Reproductive Health
  4. Obstetrics and Gynaecology
  5. Obstetrics and Gynaecology publications
Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/78852
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dc.contributor.authorJolley, A.-
dc.contributor.authorCorbett, M.-
dc.contributor.authorMcGregor, L.-
dc.contributor.authorWaters, W.-
dc.contributor.authorBrown, S.-
dc.contributor.authorNicholl, J.-
dc.contributor.authorYu, S.-
dc.date.issued2013-
dc.identifier.citationAmerican Journal of Medical Genetics Part A, 2013; 161(6):1508-1512-
dc.identifier.issn1552-4825-
dc.identifier.issn1552-4833-
dc.identifier.urihttp://hdl.handle.net/2440/78852-
dc.description.statementofresponsibilityAlexandra Jolley, Mark Corbett, Lesley McGregor, Wendy Waters, Susan Brown, Jillian Nicholl, and Sui Yu-
dc.language.isoen-
dc.publisherWiley-Liss-
dc.rightsCopyright © 2013 Wiley Periodicals, Inc.-
dc.source.urihttp://dx.doi.org/10.1002/ajmg.a.35922-
dc.subjectHumans-
dc.subjectChromosome Deletion-
dc.subjectTranslocation, Genetic-
dc.subjectProteins-
dc.subjectCytoskeletal Proteins-
dc.subjectTranscription Factors-
dc.subjectIn Situ Hybridization, Fluorescence-
dc.subjectAutistic Disorder-
dc.subjectDevelopmental Disabilities-
dc.subjectBase Sequence-
dc.subjectAdolescent-
dc.subjectMale-
dc.subjectComparative Genomic Hybridization-
dc.subjectChromosome Inversion-
dc.titleDe novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review-
dc.typeJournal article-
dc.identifier.doi10.1002/ajmg.a.35922-
pubs.publication-statusPublished-
dc.identifier.orcidCorbett, M. [0000-0001-9298-3072]-
Appears in Collections:Aurora harvest 4
Obstetrics and Gynaecology publications

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