15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH. [electronic resource]
Producer: 20060427Description: 124-34 p. digitalISSN:- 0009-9163
- Adolescent
- Adult
- Autistic Disorder -- genetics
- Child
- Chromosome Banding
- Chromosomes, Human, Pair 14 -- genetics
- Chromosomes, Human, Pair 15 -- genetics
- Family Health
- Female
- Gene Duplication
- Genome, Human
- Genomics
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Male
- Nucleic Acid Hybridization
- Pedigree
- Translocation, Genetic -- genetics
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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