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Volumn 96, Issue 5, 2015, Pages 832-840

Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; CANCER RISK; CANCER SUSCEPTIBILITY; CHINESE; CHROMOSOME 20Q; CHROMOSOME 6P; CHROMOSOME VARIANT; CONTROLLED STUDY; DNA FLANKING REGION; EXOME; FEMALE; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC CODE; GENETIC IDENTIFICATION; GENETIC MODEL; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LUNG CANCER; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; ONSET AGE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; X CHROMOSOME; Y CHROMOSOME; ASIAN CONTINENTAL ANCESTRY GROUP; CHROMOSOME 20; CHROMOSOME 6; GENETIC PREDISPOSITION; GENETICS; LUNG TUMOR; PATHOLOGY; RISK FACTOR;

EID: 84929268931     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2015.03.009     Document Type: Article
Times cited : (35)

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