Functional and clinical significance of variants localized to 8q24 in colon cancer

Cancer Epidemiology Biomarkers and Prevention

Volumn 18, Issue 9, 2009, Pages 2492-2500

  Cicek, Mine S ^a   Slager, Susan L ^a   Achenbach, Sara J ^a   French, Amy J ^a   Blair, Hilary E ^a   Fink, Stephanie R ^a   Foster, Nathan R ^a   Kabat, Brian F ^a   Halling, Kevin C ^a   Cunningham, Julie M ^a   Cerhan, James R ^a   Jenkins, Robert B ^a   Boardman, Lisa A ^a   Petersen, Gloria M ^a   Sargent, Daniel J ^a   Alberts, Steven R ^a   Limburg, Paul J ^a   Thibodeau, Stephen N ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYC PROTEIN;

ARTICLE; CANCER GROWTH; CANCER RISK; CANCER SURVIVAL; CHROMOSOME 8Q; CHROMOSOME FRAGILITY; COLON CANCER; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE FREQUENCY; GENE LOCATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 8; COLONIC NEOPLASMS; DNA MISMATCH REPAIR; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROSPECTIVE STUDIES; RISK FACTORS; SURVIVAL RATE; YOUNG ADULT;

EID: 70349313466     PISSN: 10559965     EISSN: None     Source Type: Journal    
DOI: 10.1158/1055-9965.EPI-09-0362     Document Type: Article

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