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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...
Gorde:
| Egile Nagusiak: | , , , , , , , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Oxford University Press
2013
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| Gaiak: | |
| Sarrera elektronikoa: | 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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