Pittman, Alan M <br/><br/>
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.  [electronic resource] 

 -  Human molecular genetics  Dec 2008 
 - 3720-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddn267  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Case-Control Studies<br/>Chromosomes, Human, Pair 11--genetics<br/>Colorectal Neoplasms--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Genotype<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Polymorphism, Single Nucleotide<br/>Risk Factors