Genotype and phenotype in hereditary nonpolyposis colon cancer: A study of families with different vs. shared predisposing mutations

Familial Cancer

Volumn 1, Issue 1, 2001, Pages 9-15

  Peltomäki, Päivi ^a   Gao, Xin ^a   Mecklin, Jukka Pekka ^b  

^a THE OHIO STATE UNIVERSITY COLLEGE OF MEDICINE   (United States)

^b JYVÄSKYLÄ CENTRAL HOSPITAL   (Finland)

Author keywords

DNA mismatch repair; Hereditary non polyposis colon cancer; MLH1; MSH2; Phenotypic correlations

Indexed keywords

AMINO TERMINAL SEQUENCE; ARTICLE; CANCER DIAGNOSIS; CANCER LOCALIZATION; CANCER SUSCEPTIBILITY; COLORECTAL CARCINOMA; CONTROLLED STUDY; EXON; FAMILIAL CANCER; FAMILIAL INCIDENCE; FAMILY HISTORY; FAMILY SIZE; FINLAND; GENE DELETION; GENE MUTATION; GENETIC PREDISPOSITION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MISMATCH REPAIR; MISSENSE MUTATION; ONSET AGE; PRIORITY JOURNAL;

AGED; BASE PAIR MISMATCH; CARRIER PROTEINS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA REPAIR; DNA-BINDING PROTEINS; FEMALE; FINLAND; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION; MUTS HOMOLOG 2 PROTEIN; NEOPLASM PROTEINS; NUCLEAR PROTEINS; PHENOTYPE; PROTO-ONCOGENE PROTEINS;

EID: 0035760845     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1011564720772     Document Type: Article

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