Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

Individually rare, large copy number variants (CNVs) contribute to genetic vulnerability for schizophrenia. Unresolved questions remain, however, regarding the anticipated yield of clinical microarray testing in schizophrenia. Using high-resolution genome-wide microarrays and rigorous methods, we in...

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Detalhes bibliográficos
Main Authors: Costain, Gregory, Lionel, Anath C., Merico, Daniele, Forsythe, Pamela, Russell, Kathryn, Lowther, Chelsea, Yuen, Tracy, Husted, Janice, Stavropoulos, Dimitri J., Speevak, Marsha, Chow, Eva W.C., Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3889806/
https://ncbi.nlm.nih.gov/pubmed/23813976
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt297
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