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Works
5
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability