Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype. [electronic resource]
Producer: 19981026Description: 461-7 p. digitalISSN:- 0148-7299
- Adult
- Blindness -- congenital
- Chromosome Mapping
- Chromosomes, Human, Pair 3
- Female
- Fingers -- abnormalities
- Genetic Linkage
- Haplotypes
- Humans
- Intellectual Disability -- genetics
- Intelligence Tests
- Kidney -- abnormalities
- Male
- Middle Aged
- Newfoundland and Labrador
- Obesity -- genetics
- Pedigree
- Phenotype
- Polydactyly -- genetics
- Retinitis Pigmentosa -- genetics
- Syndrome
- Toes -- abnormalities
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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