Ratings
0
Nobody has rated this yet. Be the first!
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
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
A 15q13.3 microdeletion segregating with autism
A genome-wide scan for common alleles affecting risk for autism
