Walters, R G <br/><br/>
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.  [electronic resource] 

 -  Nature  Feb 2010 
 - 671-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-4687 
<br/><br/><label>Standard No.: </label>10.1038/nature08727  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aging<br/>Body Mass Index<br/>Case-Control Studies<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 16--genetics<br/>Cognition Disorders--complications<br/>Cohort Studies<br/>Europe<br/>Female<br/>Genome-Wide Association Study<br/>Heterozygote<br/>Humans<br/>Inheritance Patterns--genetics<br/>Male<br/>Mutation--genetics<br/>Obesity--complications<br/>Penetrance<br/>Reproducibility of Results<br/>Sex Characteristics<br/>Young Adult