Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. [electronic resource]
Producer: 20060530Description: 509-14 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Apraxias -- pathology
- Child, Preschool
- Chromosome Banding
- Chromosome Deletion
- Chromosome Mapping
- Chromosomes, Human, Pair 7 -- genetics
- Female
- Forkhead Transcription Factors -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Karyotyping
- Language Disorders -- pathology
- Microsatellite Repeats -- genetics
- Speech Disorders -- pathology
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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