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Volumn 152, Issue 1, 2004, Pages 70-71

No association between two MLH3 variants (S845G and P844L)and colorectal cancer risk

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER CLASSIFICATION; CANCER RISK; COLORECTAL CANCER; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; GENE; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GERM LINE; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MLH3 GENE; PRIORITY JOURNAL;

EID: 2942556714     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2003.10.008     Document Type: Article
Times cited : (15)

References (4)
  • 2
    • 0033063711 scopus 로고    scopus 로고
    • New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC
    • Vasen H.F., Watson P., Mecklin J.P., Lynch H.T. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC. Gastroenterology. 116:1999;1453-1456
    • (1999) Gastroenterology , vol.116 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3    Lynch, H.T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.