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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease.
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot
Copy number variation in fetal alcohol spectrum disorder
Global variation in copy number in the human genome
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
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.
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