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Joder, Carmen; Gmür, Andrea; Solass, Wiebke; Christe, Lucine; Rabaglio, Manuela; Fluri, Muriel; Rau, Tilman T; Saner, Flurina A M; Knabben, Laura; Imboden, Sara; Mueller, Michael D; Siegenthaler, Franziska (2024). Real-World Data on Institutional Implementation of Screening for Mismatch Repair Deficiency and Lynch Syndrome in Endometrial Cancer Patients. Cancers, 16(3) MDPI AG 10.3390/cancers16030671
Adam, Felicia; Fluri, Muriel; Scherz, Amina; Rabaglio, Manuela (2023). Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study. BMC medical genomics, 16(1), p. 7. BioMed Central 10.1186/s12920-023-01437-7
