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Lynch syndrome
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MLH1
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Sijmons, R.H.
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(1 - 24 of 34)
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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
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants
Risk-reducing gynecological surgery in Lynch syndrome
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants
Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome
Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
Characteristics of Lynch syndrome associated ovarian cancer
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia (vol 117, pg 1215, 2017)
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
Reusability of coded data in the primary care electronic medical record: A dynamic cohort study concerning cancer diagnoses
Do GPs know their patients with cancer? Assessing the quality of cancer registration in Dutch primary care: a cross-sectional validation study
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
Do GPs know their cancer patients? A linkage study using Electronic Medical Records (EMRs)
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis
The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review
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