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Hereditary Cancer in Clinical Practice|October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumPål Møller, Toni Seppälä, James G Dowty, et al.Hereditary Cancer in Clinical Practice|November 28, 2023
Progression of duodenal neoplasia to advanced adenoma in patients with familial adenomatous polyposisHiroko Nakahira, Yoji Takeuchi, Yusaku Shimamoto, et al.Hereditary Cancer in Clinical Practice|November 18, 2023
"Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patientsJennifer L Schneider, Alison J Firemark, Sara Gille, et al.Hereditary Cancer in Clinical Practice|January 18, 2024
Li-Fraumeni syndrome presenting with de novo TP53 mutation, severe phenotype and advanced paternal age: a case reportJuan Pablo Arango-Ibañez, Luis Gabriel Parra-Lara, Ángela R Zambrano, et al.Hereditary Cancer in Clinical Practice|July 3, 2024
Two Japanese families with familial pancreatic cancer with suspected pathogenic variants of CDKN2A: a case reportYoshimi Kiyozumi, Hiroyuki Matsubayashi, Akiko Todaka, et al.Hereditary Cancer in Clinical Practice|September 3, 2024
Adrenal tumours in patients with pathogenic APC mutations: a retrospective studyLyman Lin, Victoria Beshay, Finlay MacraeHereditary Cancer in Clinical Practice|September 5, 2024
Universal screening of colorectal tumors for lynch syndrome: a survey of patient experiences and opinionsAlexander T Petterson, Jennifer Garbarini, Maria J BakerHereditary Cancer in Clinical Practice|August 27, 2024
Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional studyAlexandra Michel, Michel Dorval, Jocelyne Chiquette, et al.Hereditary Cancer in Clinical Practice|June 14, 2024
Modifiable risk factors for cancer among people with lynch syndrome: an international, cross-sectional surveyRobert F Power, Damien E Doherty, Roberta Horgan, et al.Hereditary Cancer in Clinical Practice|August 25, 2023
A novel pathogenic frameshift variant in AXIN2 in a man with polyposis and hypodontiaM F Broekema, E J W Redeker, M T Uiterwaal, et al.Pageof 48