Phenotypic variations on the theme of CNVs

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2008. Phenotypic variations on the theme of CNVs. Nature Genetics 40 (12) , pp. 1392-1393. 10.1038/ng1208-1392

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Abstract

Copy number variation has emerged as an important type of genetic risk factor for developmental disorders, including the neurodevelopmental disorders schizophrenia, autism and mental retardation. The highly pleiotropic effects observed for specific copy number variants (CNVs) challenge current classification of these disorders, but also provide opportunities to understand their origins and the relationships between them.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Medicine MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) Neuroscience and Mental Health Research Institute (NMHRI)
Subjects:	Q Science > QH Natural history > QH426 Genetics
Publisher:	Nature Publishing Group
ISSN:	1061-4036
Last Modified:	20 Oct 2022 08:59
URI:	https://orca.cardiff.ac.uk/id/eprint/30281

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