Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. [electronic resource]
Producer: 20040324Description: 311-21 p. digitalISSN:- 1098-3600
- Adolescent
- Adult
- Child
- Chromosome Mapping
- Chromosomes, Human, Pair 7
- Cohort Studies
- Cosmids
- Female
- Gene Deletion
- Gene Dosage
- Humans
- In Situ Hybridization, Fluorescence
- Intelligence Tests
- Models, Genetic
- Muscle Proteins -- genetics
- Nuclear Proteins -- genetics
- Phenotype
- Physical Chromosome Mapping
- Trans-Activators -- genetics
- Transcription Factors, TFII -- genetics
- Williams Syndrome -- diagnosis
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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