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Paper Details

Identification of rare variants from exome sequence in a large pedigree with autism.
Hum Hered
8
2012
Genome-scan marker, IVs, MYH9, autism, autism spectrum disorder, chromosome 22 region, diallelic marker panel, exome, exome sequence, haplotype, linkage marker panel, multilocus marker, rare variants, risk haplotype, sequence variants
Author NameAffiliation
Elizabeth E BlueUniversity of Washington
Elizabeth E BlueUniversity of Washington
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Datasets

Release 1.2