| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5905001 | European Journal of Medical Genetics | 2012 | 7 Pages |
Abstract
⺠Copy number variants may predispose to a range of neuropsychiatric disorders. ⺠Array CGH may reveal relevant findings in adults with complex phenotypes. ⺠Likely pathogenic copy number changes were identified with a yield of 15.6%. ⺠Array CGH should join the diagnostic repertoire for adults with complex phenotypes.
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Authors
Elizabeth C. Galizia, Maithili Srikantha, Rodger Palmer, Jonathan J. Waters, Nicholas Lench, Caroline Mackie Ogilvie, Dalia KasperaviÄiÅ«tÄ, Lina Nashef, Sanjay M. Sisodiya,