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Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV
Recurrent deletions and duplications at chromosomal region 16p11.2 are a major genetic contributor to autism but also associate with a wider range of pediatric diagnoses, including intellectual disability, coordination disorder, and language disorder. In order to investigate the potential genetic ba...
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| Veröffentlicht in: | Am J Hum Genet |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4716684/ https://ncbi.nlm.nih.gov/pubmed/26749307 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2015.11.017 |
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