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Functional impact of global rare copy number variation in 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
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
