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Adult Neuropsychiatric Expression and Familial Segregation of 2q13 Duplications
New genomic disorders associated with large, rare, recurrent copy number variations (CNVs) are being discovered at a rapid pace. Detailed phenotyping and family studies are rare, however, as are data on adult phenotypic expression. Duplications at 2q13 were recently identified as risk factors for de...
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| Vydáno v: | Am J Med Genet B Neuropsychiatr Genet |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4464821/ https://ncbi.nlm.nih.gov/pubmed/24807792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32236 |
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