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Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment
No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2
Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants
The management of Peutz-Jeghers syndrome: European Hereditary Tumour Group (EHTG) guideline
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants
The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance
Associations of pathogenic variants in MLH1, MSH2, and MSH6 with risk of colorectal adenomas and tumors and with somatic mutations in patients with Lynch syndrome
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants
The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis
Deciphering the Colon Cancer Genes-Report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010
How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010
Peutz-Jeghers syndrome: a systematic review and recommendations for management
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe