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Individual common variants exert weak effects on the risk for autism spectrum disorders
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
A 15q13.3 microdeletion segregating with autism
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
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
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
