| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1002/(SICI)1097-0215(19960220)69:1<38::AID-IJC9>3.0.CO;2-X |
| P698 | PubMed publication ID | 8600057 |
| P2093 | author name string | H T Lynch | |
| T Smyrk | |||
| J F Lynch | |||
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| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | molecular genetics | Q210506 |
| Lynch syndrome | Q783644 | ||
| P1104 | number of pages | 6 | |
| P304 | page(s) | 38-43 | |
| P577 | publication date | 1996-02-01 | |
| P1433 | published in | International Journal of Cancer | Q332492 |
| P1476 | title | Overview of natural history, pathology, molecular genetics and management of HNPCC (Lynch Syndrome). | |
| P478 | volume | 69 |
| Q33685993 | A practical approach to familial and hereditary colorectal cancer |
| Q34067753 | Approaching the adnexal mass in the new millennium |
| Q35079926 | BRCA2 and pancreatic cancer |
| Q36084326 | Biomarkers in endometrial cancer: Possible clinical applications (Review) |
| Q61917173 | Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer |
| Q42134566 | Choice of management strategy for colorectal cancer based on a diagnostic immunohistochemical test for defective mismatch repair |
| Q52893411 | DNA mismatch repair in lymphoblastoid cells from hereditary non-polyposis colorectal cancer (HNPCC) patients is normal under conditions of rapid cell division and increased mutational load. |
| Q41536289 | DNA mismatch repair in mammals: role in disease and meiosis |
| Q48682503 | Disease expression in Swiss hereditary non-polyposis colorectal cancer (HNPCC) kindreds |
| Q34615912 | Distinction between familial and sporadic forms of colorectal cancer showing DNA microsatellite instability |
| Q33839135 | Epidemiology and molecular genetics of colorectal cancer |
| Q77924565 | Epithelial ovarian cancer |
| Q36421123 | Exonuclease 1 (Exo1) is required for activating response to S(N)1 DNA methylating agents |
| Q89849938 | Expanding the Scope of Immunotherapy in Colorectal Cancer: Current Clinical Approaches and Future Directions |
| Q36641429 | Extensive molecular screening for hereditary non-polyposis colorectal cancer |
| Q41955895 | FAP: another indication to treat H pylori |
| Q36294972 | Family history of cancer and risk of colorectal cancer in Italy |
| Q57560315 | Family history of cancer and risk of ovarian cancer |
| Q35840995 | Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas |
| Q36318595 | From gene mutations to tumours--stem cells in gastrointestinal carcinogenesis. |
| Q47713981 | Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae |
| Q36672157 | Gastrointestinal stem cells and cancer: bridging the molecular gap. |
| Q35034265 | Genetic testing for colon cancer: joint statement of the American College of Medical Genetics and American Society of Human Genetics. Joint Test and Technology Transfer Committee Working Group |
| Q35810149 | Genetic, immunohistochemical, and clinical features of medullary carcinoma of the pancreas: A newly described and characterized entity |
| Q43869182 | Germ cells microsatellite instability. The effect of different mutagens in a mismatch repair mutant of Drosophila (spel1). |
| Q42005199 | Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer |
| Q52551102 | Germline mutations at microsatellite loci in homozygous and heterozygous mutants for mismatch repair and PCNA genes in Drosophila. |
| Q53600496 | How cancer gene testing can benefit patients. |
| Q40762811 | Identification and functional characterization of the promoter region of the human MSH6 gene |
| Q57742300 | Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22 |
| Q79156469 | Laparoscopic prophylactic surgery for HNPCC gene mutation carrier: has the time come? |
| Q28131788 | Lessons from hereditary colorectal cancer |
| Q43235852 | Macrocyclic DNA-mismatch-binding ligands: structural determinants of selectivity |
| Q36660380 | Microsatellite instability status in gastric cancer: a reappraisal of its clinical significance and relationship with mucin phenotypes |
| Q36618286 | Microsatellite instability, Epstein-Barr virus, mutation of type II transforming growth factor beta receptor and BAX in gastric carcinomas in Hong Kong Chinese |
| Q26764919 | Molecular alterations in gastric cancer with special reference to the early-onset subtype |
| Q33540554 | Molecular genetics of gastrointestinal malignancies |
| Q33368199 | Molecular pathogenesis of colorectal cancer |
| Q36325598 | Mouse embryonic stem cells carrying one or two defective Msh2 alleles respond abnormally to oxidative stress inflicted by low-level radiation |
| Q36417805 | Mutational targets in colorectal cancer cells with microsatellite instability. |
| Q33347546 | Nature meets nurture: molecular genetics of gastric cancer. |
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| Q35765148 | Pancreatic adenocarcinomas with DNA replication errors (RER+) are associated with wild-type K-ras and characteristic histopathology. Poor differentiation, a syncytial growth pattern, and pushing borders suggest RER+ |
| Q35594437 | Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing |
| Q36404900 | Pathologic predictors of microsatellite instability in colorectal cancer |
| Q34102606 | Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study |
| Q41563180 | Preoperative and postoperative imaging for colorectal cancer |
| Q33493198 | Presence of activating KRAS mutations correlates significantly with expression of tumour suppressor genes DCN and TPM1 in colorectal cancer |
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