Wang, Xianshu <br/><br/>
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.  [electronic resource] 

 -  Human molecular genetics  Jul 2010 
 - 2886-97 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddq174  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Breast Neoplasms--genetics<br/>Carcinoma--genetics<br/>Epistasis, Genetic--physiology<br/>Female<br/>Gene Frequency<br/>Genes, BRCA1<br/>Genes, BRCA2<br/>Genetic Loci--physiology<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Middle Aged<br/>Mutation--physiology<br/>Polymorphism, Single Nucleotide--physiology<br/>Risk Factors