Contribution of the FMR1 gene mutation to human intellectual dysfunction. [electronic resource]
Producer: 19951208Description: 331-4 p. digitalISSN:- 1061-4036
- Adolescent
- Case-Control Studies
- Child
- Dosage Compensation, Genetic
- Female
- Fragile X Mental Retardation Protein
- Fragile X Syndrome -- genetics
- Humans
- Intellectual Disability -- genetics
- Intelligence -- genetics
- Intelligence Tests
- Mutation
- Nerve Tissue Proteins -- genetics
- Parents
- RNA-Binding Proteins
- Regression Analysis
- Repetitive Sequences, Nucleic Acid
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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