Recurrent 16p11.2 microdeletions in autism. [electronic resource]
Producer: 20080312Description: 628-38 p. digitalISSN:- 1460-2083
- Autistic Disorder -- genetics
- Base Sequence
- Case-Control Studies
- Child
- Chromosome Breakage
- Chromosome Deletion
- Chromosomes, Artificial, Bacterial -- genetics
- Chromosomes, Human, Pair 16 -- genetics
- DNA Primers -- genetics
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Microsatellite Repeats
- Pedigree
- Phenotype
- Polymerase Chain Reaction
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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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