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Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, ISSN 1542-3565, 07/2019
Lynch syndrome is the most common inherited cause of gastrointestinal cancer and increases risk for a variety of malignancies, including gastric cancer. We... 
Journal Article
GENETICS IN MEDICINE, ISSN 1098-3600, 01/2009, Volume 11, Issue 1, pp. 35 - 41
Of Recommendations: The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group found sufficient evidence to recommend offering... 
HNPCC | COST-EFFECTIVENESS | colorectal cancer | FAMILIES | GENETICS & HEREDITY | SURVEILLANCE | RISK | TERM | CARCINOMA | CARRIERS | Lynch syndrome
Journal Article
Human Pathology, ISSN 0046-8177, 02/2019, Volume 84, pp. 299 - 308
Colorectal cancer (CRC) is a neoplastic disease in which normal mucosa undergoes a process of malignant transformation due to the progressive accumulation of... 
β-catenin | Ki-67 | Hereditary nonpolyposis colorectal cancer (HNPCC) | Wnt pathway | Sporadic CRC | Cadherin | Hereditary CRC | Epigenetics | Mutation | Medical prognosis | Genes | Cancer | Tumors
Journal Article
Journal Article
Cancer Cell, ISSN 1535-6108, 2011, Volume 20, Issue 2, pp. 200 - 213
Constitutional epimutations of tumor suppressor genes manifest as promoter methylation and transcriptional silencing of a single allele in normal somatic... 
HNPCC | LYNCH-SYNDROME | HYPERMETHYLATION | DNA METHYLATION | GENE | ONCOLOGY | NONPOLYPOSIS COLORECTAL-CANCER | PROMOTER METHYLATION | MICROSATELLITE INSTABILITY | GERMLINE EPIMUTATIONS | MUTATIONS | CELL BIOLOGY
Journal Article
Gastroenterology, ISSN 0016-5085, 05/2019, Volume 156, Issue 6, pp. 1924 - 1925.e4
Journal Article
Gut, ISSN 0017-5749, 06/2013, Volume 62, Issue 6, pp. 812 - 823
Journal Article
Gut, ISSN 0017-5749, 09/2013, Volume 62, Issue 9, pp. 1315 - 1326
Journal Article
Journal Article
BMB Reports, ISSN 1976-6696, 2011, Volume 44, Issue 5, pp. 317 - 322
Hereditary non-polyposis Colorectal Cancer (HNPCC) is an autosomal dominant inheritance syndrome. HNPCC is the most common hereditary variant of colorectal... 
HNPCC | Mutations | MSH2 | MLH1
Journal Article
HUMAN PATHOLOGY, ISSN 0046-8177, 02/2019, Volume 84, pp. 299 - 308
Colorectal cancer (CRC) is a neoplastic disease in which normal mucosa undergoes a process of malignant transformation due to the progressive accumulation of... 
beta-catenin | Ki-67 | PROFILE | Hereditary nonpolyposis colorectal cancer (HNPCC) | Wnt pathway | PATHWAY | MARKERS | Sporadic CRC | COLON | PATHOLOGY | Cadherin | Hereditary CRC
Journal Article