Young, T L <br/><br/>
Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.  [electronic resource] 

 -  American journal of medical genetics  Aug 1998 
 - 461-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1096-8628(19980806)78:5<461::aid-ajmg12>3.0.co;2-d  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Blindness--congenital<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 3<br/>Female<br/>Fingers--abnormalities<br/>Genetic Linkage<br/>Haplotypes<br/>Humans<br/>Intellectual Disability--genetics<br/>Intelligence Tests<br/>Kidney--abnormalities<br/>Male<br/>Middle Aged<br/>Newfoundland and Labrador<br/>Obesity--genetics<br/>Pedigree<br/>Phenotype<br/>Polydactyly--genetics<br/>Retinitis Pigmentosa--genetics<br/>Syndrome<br/>Toes--abnormalities