Ghorbanoghli, Z <br/><br/>
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.  [electronic resource] 

 -  Familial cancer  10 2016 
 - 563-70 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1573-7292 
<br/><br/><label>Standard No.: </label>10.1007/s10689-016-9877-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenoma--genetics<br/>Adenomatous Polyposis Coli--genetics<br/>Adenomatous Polyposis Coli Protein--genetics<br/>Adult<br/>Chromosomes, Human, Pair 11<br/>Chromosomes, Human, Pair 8<br/>Colorectal Neoplasms--genetics<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Humans<br/>Male<br/>Mutation<br/>Polymorphism, Single Nucleotide