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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Autores principales: 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
Lenguaje:Inglês
Publicado: Oxford University Press 2013
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Articles
Acceso en línea: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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