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Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
22q11.2 Deletion Syndrome (22q11.2DS) is a common microdeletion syndrome with congenital and late-onset features. Testing for the genomic content of copy number variations (CNVs) may help elucidate the 22q11.2 deletion mechanism and the variable clinical expression of the syndrome including the high...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2008
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2638574/ https://ncbi.nlm.nih.gov/pubmed/18806272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn307 |
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