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Paper Details

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
J Med Genet
75
2011
1, 16q21 microdeletions, ASD, Autism spectrum disorder, CDH8, CDH8 isoforms, CNVs, LD, SNP array, autism, boys, cadherin 8, chr16: 58724527-60547472, chr16: 60025584-61667839, chromosome 16q21, copy number variations, familial, familial 16q21 microdeletions, genomic variants, human, learning disability, linkage region, reverse transcriptase

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Release 1.2