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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
