Lynch syndrome: toward an increasingly complex picture. The case of PMS2
Author:
Affiliation:
1. Division of Cancer Prevention and Genetics, IEO, European Institute of Oncology, IRCCS, Milan, Italy
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cancer Research,Public Health, Environmental and Occupational Health,Oncology,Epidemiology
Reference10 articles.
1. The coding microsatellite mutation profile of PMS2-deficient colorectal cancer.;Bajwa-Ten Broeke;Exp Mol Pathol,2021
2. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium.;Bakry;Eur J Cancer (Oxford, England: 1990),2014
3. Exome sequencing in a Swedish family with PMS2 mutation with varying penetrance of colorectal cancer: investigating the presence of genetic risk modifiers in colorectal cancer risk.;Bryant;Eur J Cancer Prev,2023
4. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.;Dominguez-Valentin;Genet Med,2020
5. No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2: a prospective Lynch syndrome database study.;Dominguez-Valentin;J Clin Med,2021
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