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Genes, Chromosomes & Cancer|March 10, 2018
Evaluation of MLH1 variants of unclear significanceNicole Köger, Lea Paulsen, Francisco López-Kostner, et al.
Familial Cancer|June 18, 2011
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individualsMev Dominguez Valentin, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, et al.
Gynecologic Oncology|August 10, 2025
Ovarian cancer after breast cancer in women with a BRCA1 or BRCA2 pathogenic variantAdriana I Apostol, Joanne Kotsopoulos, Jacek Gronwald, et al.
Genes, Chromosomes & Cancer|May 9, 2024
Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndromeAnne-Sophie van der Werf-'t Lam, Mar Rodriguez-Girondo, Mandy Villasmil, et al.
Familial Cancer|May 5, 2020
MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicingTamara Alejandra Piñero, Omar Soukarieh, Marion Rolain, et al.
International Journal of Cancer|July 20, 2020
The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillanceAysel Ahadova, Toni T Seppälä, Christoph Engel, et al.
European Journal of Cancer (Oxford, England : 1990)|May 6, 2026
ESGO Consensus Statement on endometrial cancer prevention, risk reduction strategies, and management of women with Lynch syndromeClaudia Marchetti, Murat Gultekin, Carolina Maria Sassu, et al.
International Journal of Cancer|October 10, 2022
Is HLA type a possible cancer risk modifier in Lynch syndrome?Aysel Ahadova, Johannes Witt, Saskia Haupt, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Analysis of structure and conservation for supporting functional evaluation of PMS2 missense variantsNicholas Zeuzem, Manon Quilan, Mev Dominguez-Valentin, et al.
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