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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Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2013
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On-line přístup: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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