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Familial Cancer|July 21, 2020
Multiple primary cancers (renal papillary, lymphoma and teratoma) and hepatic cysts in association with a pathogenic germline mutation in the MET geneJulian Adlard
Familial Cancer|November 25, 2025
Pancreatic cancer surveillance not recommended for familial adenomatous polyposis: a fine and gray risk analysisAleksander M Bogdanski, Derk C F Klatte, Sobia I Laghari, et al.
Familial Cancer|November 26, 2025
Updated genetic testing in individuals with unexplained adenomatous polyposis and the diagnostic yieldBlake Rowell, Maegan E Roberts, Pamela L Brock, et al.
Familial Cancer|January 6, 2026
Beyond 1100delC: distinct CHEK2 variants and unique cancer phenotypes in Northeast BrazilMariana Macambira Noronha, Pedro Robson Costa Passos, Valbert Oliveira Costa Filho, et al.
Familial Cancer|October 29, 2025
History and clinical epidemiology of NF2-related schwannomatosisD Gareth Evans, Jaishri O Blakeley, Scott R Plotkin
Familial Cancer|October 7, 2025
Reclassification of an uncertain STK11 germline variant as likely pathogenic: a family studyLorena Moreno, Miriam Cuatrecasas, Elia Grau, et al.
Familial Cancer|May 10, 2020
Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinicsB Meiser, R Kaur, J Kirk, et al.
Familial Cancer|April 25, 2020
Primary fallopian tube carcinoma (PFTC) in a BRIP-1 mutation carrier: the first case reportGiovanni Grandi, Martina Caroli, Carlo Alboni, et al.
Familial Cancer|September 17, 2025
Cancer spectrum in Mexican patients with the CHEK2 p.(Leu236Pro) variant: a retrospective studyL Leonardo Flores-Lagunes, Rosa María Alvarez-Gómez, Carolina Molina-Garay, et al.
Familial Cancer|August 11, 2025
Parental perspectives on the use of tumor molecular profiling and germline genetic testing during their children's cancer treatmentMarcelo M Sleiman, Muriel R Statman, Mary Rose Yockel, et al.
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