Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders. [electronic resource]
Producer: 20150212Description: 71-8 p. digitalISSN:- 1476-5438
- Adolescent
- Child
- Child Development Disorders, Pervasive -- etiology
- Child, Preschool
- Chromosomes, Human, Pair 15 -- genetics
- Chromosomes, Human, Pair 5 -- genetics
- Comparative Genomic Hybridization
- Cri-du-Chat Syndrome -- genetics
- DNA Copy Number Variations -- genetics
- DNA Methylation -- genetics
- Female
- Genetic Association Studies
- Genotype
- Humans
- Infant
- Male
- Oligonucleotide Array Sequence Analysis -- methods
- Polymorphism, Single Nucleotide -- genetics
- Trisomy -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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