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Works
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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
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
