Hamdi, Yosr <br/><br/>
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.  [electronic resource] 

 -  Breast cancer research and treatment  01 2017 
 - 117-134 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1573-7217 
<br/><br/><label>Standard No.: </label>10.1007/s10549-016-4018-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Biomarkers, Tumor<br/>Breast Neoplasms--epidemiology<br/>Chromosomes, Human, Pair 11<br/>Female<br/>Gene Expression<br/>Genes, BRCA1<br/>Genes, BRCA2<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Heterozygote<br/>Humans<br/>Mutation<br/>Quantitative Trait Loci<br/>Risk