Identification of germline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer

Cancer Genetics and Cytogenetics

Volumn 146, Issue 1, 2003, Pages 58-65

  Banno, Kouji ^a   Susumu, Nobuyuki ^a   Hirao, Takeshi ^a   Yanokura, Megumi ^a   Hirasawa, Akira ^a   Aoki, Daisuke ^a   Udagawa, Yasuhiro ^b   Sugano, Kokichi ^c   Nozawa, Shiro ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c TOCHIGI CANCER CENTER   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CODON; COLORECTAL CARCINOMA; CONTROLLED STUDY; ENDOMETRIUM CARCINOMA; FAMILY HISTORY; FEMALE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GERM LINE; HUMAN; HUMAN TISSUE; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; MISSENSE MUTATION; MSH2 GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0141565164     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(03)00157-2     Document Type: Article

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