| Keywords: |
gene mutation; single nucleotide polymorphism; polymorphism, single nucleotide; nuclear magnetic resonance imaging; heredity; genetic predisposition to disease; chemoprophylaxis; breast cancer; prevalence; tumor markers, biological; genotype; gene frequency; transcription factor; editorial; breast neoplasms; cancer research; risk factor; prostate cancer; genome analysis; homozygosity; oncogene; heterozygosity; colon cancer; genetic susceptibility; predictive value of tests; pregnancy; binding site; receptors, estrogen; cancer epidemiology; estrogen receptor; european continental ancestry group; chromosome 2; carcinoma, intraductal, noninfiltrating; genetic heterogeneity; neoplasms, hormone-dependent; attributable risk; genetic epidemiology; asian continental ancestry group; carcinoma, ductal, breast
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