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| Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. |
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| Functional impact of global rare copy number variation in autism spectrum disorders. |
2010 |
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| Structural variation of chromosomes in autism spectrum disorder. |
2008 |
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| Contribution of SHANK3 mutations to autism spectrum disorder. |
2007 |
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| Mapping autism risk loci using genetic linkage and chromosomal rearrangements. |
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