1. Adelaide Research & Scholarship
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  3. School of Paediatrics & Reproductive Health
  4. Paediatrics
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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/72328
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dc.contributor.authorVoineagu, J.-
dc.contributor.authorHuang, L.-
dc.contributor.authorWinden, K.-
dc.contributor.authorLazaro, M.-
dc.contributor.authorHaan, E.-
dc.contributor.authorNelson, J.-
dc.contributor.authorMcGaughran, J.-
dc.contributor.authorNguyen, L.-
dc.contributor.authorFriend, K.-
dc.contributor.authorHackett, A.-
dc.contributor.authorField, M.-
dc.contributor.authorGecz, J.-
dc.contributor.authorGeschwind, D.-
dc.date.issued2012-
dc.identifier.citationMolecular Psychiatry, 2012; 17(1):4-7-
dc.identifier.issn1359-4184-
dc.identifier.issn1476-5578-
dc.identifier.urihttp://hdl.handle.net/2440/72328-
dc.descriptionLetter to the editor-
dc.description.statementofresponsibilityI Voineagu, L Huang, K Winden, M Lazaro, E Haan, J Nelson, J McGaughran, LS Nguyen, K Friend, A Hackett, M Field, J Gecz and D Geschwind-
dc.language.isoen-
dc.publisherNature Publishing Group-
dc.rightsCopyright status unknown-
dc.source.urihttp://dx.doi.org/10.1038/mp.2011.95-
dc.subjectChromosomes, Human, X-
dc.subjectHumans-
dc.subjectGenetic Diseases, X-Linked-
dc.subjectGenetic Predisposition to Disease-
dc.subjectProteins-
dc.subjectCarrier Proteins-
dc.subjectDNA-Binding Proteins-
dc.subjectNuclear Proteins-
dc.subjectRNA, Messenger-
dc.subjectCase-Control Studies-
dc.subjectCohort Studies-
dc.subjectPhenotype-
dc.subjectMutation-
dc.subjectMale-
dc.subjectGenome-Wide Association Study-
dc.subjectIntellectual Disability-
dc.titleCCDC22: a novel candidate gene for syndromic X-linked intellectual disability-
dc.typeJournal article-
dc.identifier.doi10.1038/mp.2011.95-
pubs.publication-statusPublished-
dc.identifier.orcidHaan, E. [0000-0002-7310-5124]-
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]-
Appears in Collections:Aurora harvest
Paediatrics publications

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