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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
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Cost Offset Associated With Early Start Denver Model for Children With Autism.
A genome-wide scan for common alleles affecting risk for autism
