Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts. [electronic resource]
Producer: 20140529Description: 1090-5 p. digitalISSN:- 1476-5578
- Autistic Disorder -- epidemiology
- Causality
- Child Development Disorders, Pervasive -- epidemiology
- Congenital Abnormalities -- epidemiology
- Data Mining
- Developmental Disabilities -- epidemiology
- Gene Deletion
- Gene Dosage
- Gene Duplication
- Genetic Association Studies
- Genetic Heterogeneity
- Genetic Predisposition to Disease
- Homologous Recombination
- Humans
- Prevalence
- Sample Size
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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