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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Bibliografische gegevens
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2013
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Articles
Online toegang: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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