| Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. |
2013 |
24076603 |
| 11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity. |
2011 |
21567907 |
| Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. |
2011 |
21658581 |
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