Association of genetic polymorphisms and haplotypes in hMLH1 and hMSH3 gene with the risk of papillary thyroid carcinoma

Chinese Journal of Medical Genetics

Volumn 25, Issue 4, 2008, Pages 390-395

  Shi, Wen Ping ^a   Bian, Jian Chao ^b   Jiang, Feng ^b   Ni, Hong Xia ^b   Zhu, Qian Xi ^b   Tang, Hong Wei ^b   Shen, Qiang ^b   Wu, Yi ^b  

^a Minhang District Center for Disease Control and Prevention   (China)

^b FUDAN UNIVERSITY   (China)

Author keywords

Genetic polymorphism; Haplotype; hMLH1 gene; hMSH3 gene; Papillary thyroid carcinoma

Indexed keywords

ARTICLE; CHINESE; CONFIDENCE INTERVAL; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC SCREENING; GENOTYPE; HAPLOTYPE; HMLH1 GENE; HMSH3 GENE; HUMAN; MUTANT; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RISK FACTOR; STATISTICAL SIGNIFICANCE; THYROID CARCINOMA;

ADENOCARCINOMA, PAPILLARY; ADULT; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK; THYROID NEOPLASMS;

EID: 50249133211     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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