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Volumn 51, Issue 10, 2010, Pages 1870-1874
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Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence
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Author keywords
acute lymphoblastic leukemia; Polymorphism; risk
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Indexed keywords
ACUTE LYMPHOBLASTIC LEUKEMIA;
ARTICLE;
CANCER INCIDENCE;
CANCER RISK;
CAUCASIAN;
CHILD;
CHROMOSOME 10Q;
CHROMOSOME 14Q;
CHROMOSOME 7P;
CHROMOSOME 9P;
CONTROLLED STUDY;
FEMALE;
GENE FREQUENCY;
GENE LINKAGE DISEQUILIBRIUM;
GENETIC ASSOCIATION;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
PRE B LYMPHOCYTE;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
RACE DIFFERENCE;
RISK ASSESSMENT;
SINGLE NUCLEOTIDE POLYMORPHISM;
STATISTICAL ANALYSIS;
THAILAND;
ADOLESCENT;
ADULT;
ASIAN CONTINENTAL ANCESTRY GROUP;
CASE-CONTROL STUDIES;
CHILD;
CHROMOSOMES, HUMAN, PAIR 10;
CHROMOSOMES, HUMAN, PAIR 7;
EUROPEAN CONTINENTAL ANCESTRY GROUP;
FEMALE;
GENE FREQUENCY;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HUMANS;
INCIDENCE;
LINKAGE DISEQUILIBRIUM;
MALE;
POLYMORPHISM, SINGLE NUCLEOTIDE;
PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;
RISK FACTORS;
THAILAND;
YOUNG ADULT;
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EID: 77957735025
PISSN: 10428194
EISSN: 10292403
Source Type: Journal
DOI: 10.3109/10428194.2010.511356 Document Type: Article |
Times cited : (43)
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References (11)
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