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Works
6
Functional impact of global rare copy number variation in autism spectrum disorders
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Individual common variants exert weak effects on the risk for autism spectrum disorders
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
A genome-wide scan for common alleles affecting risk for autism
