Replication of the 10q11 and Xp11 prostate cancer risk variants: Results from a Utah pedigree-based study

Cancer Epidemiology Biomarkers and Prevention

Volumn 18, Issue 4, 2009, Pages 1290-1294

  Camp, Nicola J ^a,b   Farnham, James M ^a   Wong, Jathine ^a   Christensen, G Bryce ^a   Thomas, Alun ^a   Cannon Albright, Lisa A ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CANCER RISK; CANCER SUSCEPTIBILITY; CASE CONTROL STUDY; CHROMOSOME 10Q; CHROMOSOME XP; CONTROLLED STUDY; CORRELATION ANALYSIS; FAMILIAL CANCER; GENE FREQUENCY; GENE LOCUS; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HIGH RISK POPULATION; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PEDIGREE; PRIORITY JOURNAL; PROSTATE CANCER; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED STATES;

AGED; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, X; COHORT STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; MALE; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROSTATIC NEOPLASMS; RISK FACTORS; UTAH;

EID: 66649133395     PISSN: 10559965     EISSN: None     Source Type: Journal    
DOI: 10.1158/1055-9965.EPI-08-0327     Document Type: Article

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