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Journal of Medical Genetics|June 5, 2010
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypesMarielle W G Ruijs, Senno Verhoef, Matti A Rookus, et al.Journal of Human Genetics|January 4, 2023
Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 geneIrma van de Beek, Iris E Glykofridis, Michael W T Tanck, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 24, 2012
Risks of less common cancers in proven mutation carriers with lynch syndromeChristoph Engel, Markus Loeffler, Verena Steinke, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 19, 2006
Frequency and spectrum of cancers in the Peutz-Jeghers syndromeNicholas Hearle, Valérie Schumacher, Fred H Menko, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 17, 2014
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer riskSanne W ten Broeke, Richard M Brohet, Carli M Tops, et al.Gastroenterology|November 18, 2008
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndromeJuul T Wijnen, Richard M Brohet, Ronald van Eijk, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2015
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriersManon Suerink, Heleen M van der Klift, Sanne W Ten Broeke, et al.Journal of Medical Genetics|February 27, 2023
Update of penetrance estimates in Birt-Hogg-Dubé syndromeFiona Jane Bruinsma, James G Dowty, Aung Ko Win, et al.American Journal of Obstetrics and Gynecology|January 25, 2021
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort studyLieske H Schrijver, Antonis C Antoniou, Håkan Olsson, et al.Pageof 7