TY  - GEN
AU  - Young,T L
AU  - Woods,M O
AU  - Parfrey,P S
AU  - Green,J S
AU  - O'Leary,E
AU  - Hefferton,D
AU  - Davidson,W S
TI  - Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype
SN  - 0148-7299
PY  - 1998///1026
KW  - Adult
KW  - Blindness
KW  - congenital
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 3
KW  - Female
KW  - Fingers
KW  - abnormalities
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Humans
KW  - Intellectual Disability
KW  - genetics
KW  - Intelligence Tests
KW  - Kidney
KW  - Male
KW  - Middle Aged
KW  - Newfoundland and Labrador
KW  - Obesity
KW  - Pedigree
KW  - Phenotype
KW  - Polydactyly
KW  - Retinitis Pigmentosa
KW  - Syndrome
KW  - Toes
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/(sici)1096-8628(19980806)78:5<461::aid-ajmg12>3.0.co;2-d
ER  -