review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1038/NCPGASTHEP1235 |
P698 | PubMed publication ID | 18797444 |
P2093 | author name string | Wendy S Rubinstein | |
Scott M Weissman | |||
P2860 | cites work | Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability | Q24618618 |
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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene | Q33904639 | ||
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome | Q33904733 | ||
Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2 | Q33910123 | ||
MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancer | Q57200538 | ||
Accuracy of Colorectal Polyp Self-Reports: Findings from the Colon Cancer Family Registry | Q57268364 | ||
Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22 | Q57742300 | ||
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Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008 | Q60016790 | ||
Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome | Q60167349 | ||
Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas | Q61195948 | ||
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MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancers | Q74455966 | ||
Practice parameters for the identification and testing of patients at risk for dominantly inherited colorectal cancer | Q74615205 | ||
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The "duty to warn" a patient's family members about hereditary disease risks | Q80597182 | ||
Microsatellite instability is frequently observed in rectal cancer and influenced by neoadjuvant chemoradiation | Q80734818 | ||
Molecular screening for the Lynch syndrome--better than family history? | Q81716567 | ||
Hereditary colorectal cancer: risk assessment and management | Q34045183 | ||
Deficient DNA mismatch repair: a common etiologic factor for colon cancer | Q34189020 | ||
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Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer | Q35443388 | ||
Attenuated familial adenomatous polyposis (AFAP). A review of the literature | Q35566208 | ||
Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability | Q35747961 | ||
The multiple colorectal adenoma phenotype and MYH, a base excision repair gene | Q35854432 | ||
Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history | Q35895179 | ||
Phenotypic characteristics and risk of cancer development in hyperplastic polyposis: case series and literature review | Q35901489 | ||
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors | Q35986971 | ||
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The hamartomatous polyposis syndromes: a clinical and molecular review | Q36018533 | ||
Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations | Q36338216 | ||
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Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review | Q36604730 | ||
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Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function | Q43146864 | ||
Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutations | Q43915120 | ||
Gynecologic cancer prevention in Lynch syndrome/hereditary nonpolyposis colorectal cancer families | Q46153060 | ||
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States | Q46655105 | ||
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P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | gastroenterology | Q120569 |
P304 | page(s) | 569-582 | |
P577 | publication date | 2008-09-16 | |
P1433 | published in | Nature Reviews Gastroenterology & Hepatology | Q2108255 |
P1476 | title | Managing hereditary gastrointestinal cancer syndromes: the partnership between genetic counselors and gastroenterologists | |
P478 | volume | 5 |
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Q21261903 | Duodenal carcinoma at the ligament of Treitz. A molecular and clinical perspective |
Q55717557 | Frontiers in Gastrointestinal Oncology: Advances in Multi-Disciplinary Patient Care. |
Q42434480 | Signs and genetics of rare cancer syndromes with gastroenterological features |
Q34081267 | The genetic basis of Lynch syndrome and its implications for clinical practice and risk management |
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