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Strong association of de novo copy number mutations with autism.
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Copy-number variations associated with autism spectrum disorder.
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Autism-like atypical face processing in mutant dogs.
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Role of androgen receptors in sexually dimorphic phenotypes in UBE3A-dependent autism spectrum disorder.
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本文引用的文献

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Structural variation of chromosomes in autism spectrum disorder.
Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009. Epub 2008 Jan 17.
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Association between microdeletion and microduplication at 16p11.2 and autism.
N Engl J Med. 2008 Feb 14;358(7):667-75. doi: 10.1056/NEJMoa075974. Epub 2008 Jan 9.
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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015.
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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.
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Recurrent 16p11.2 microdeletions in autism.
Hum Mol Genet. 2008 Feb 15;17(4):628-38. doi: 10.1093/hmg/ddm376. Epub 2007 Dec 21.
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Correction of fragile X syndrome in mice.
Neuron. 2007 Dec 20;56(6):955-62. doi: 10.1016/j.neuron.2007.12.001.
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Gene expression changes in children with autism.
Genomics. 2008 Jan;91(1):22-9. doi: 10.1016/j.ygeno.2007.09.003. Epub 2007 Nov 14.
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Contribution of SHANK3 mutations to autism spectrum disorder.
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