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Volumn 21, Issue 31, 2015, Pages 9253-9261

Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer

Author keywords

Constitutional mismatch repair deficiency syndrome; DNA mismatch repair; Familial colorectal cancer; Familial colorectal cancer type X; Hereditary colorectal cancer; Hereditary non polyposis colorectal cancer; Lynch syndrome; Lynch like syndrome; Microsatellite instability

Indexed keywords

ARTICLE; CANCER DIAGNOSIS; CANCER PATIENT; CANCER RISK; DIFFERENTIAL DIAGNOSIS; DISEASE SURVEILLANCE; DNA STRAND; ENDOMETRIUM CANCER; FAMILIAL COLORECTAL CANCER TYPE X SYNDROME; GENE DELETION; GENE INSERTION; GENETIC PREDISPOSITION; GERMLINE MUTATION; HEREDITARY BREAST AND OVARIAN CANCER SYNDROME; HEREDITARY COLORECTAL CANCER; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HUMAN; IMMUNOHISTOCHEMISTRY; INDEL MUTATION; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; NEXT GENERATION SEQUENCING; PHENOTYPE; POINT MUTATION; POLYMERASE PROOFREADING ASSOCIATED POLYPOSIS SYNDROME; PROTEIN EXPRESSION; RISK ASSESSMENT; SOMATIC MUTATION; BRAIN TUMOR; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; COLORECTAL TUMOR; DNA MUTATIONAL ANALYSIS; GENETICS; HEREDITARY TUMOR; HEREDITY; MUTATION; PEDIGREE; PREDICTIVE VALUE;

EID: 84940056796     PISSN: 10079327     EISSN: 22192840     Source Type: Journal    
DOI: 10.3748/wjg.v21.i31.9253     Document Type: Article
Times cited : (143)

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