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Hereditary Cancer in Clinical Practice|November 22, 2017
The BRCA2 variant c.68-7 T>A is associated with breast cancerPål Møller, Eivind HovigHereditary Cancer in Clinical Practice|October 7, 2016
Prevalence of the CHEK2 R95* germline mutationStian Knappskog, Beryl Leirvaag, Liv B Gansmo, et al.Hereditary Cancer in Clinical Practice|March 11, 2014
Colorectal cancer and self-reported tooth agenesisNoralane M Lindor, Aung Ko Win, Steven Gallinger, et al.Hereditary Cancer in Clinical Practice|January 19, 2017
Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancerWenche Listøl, Hildegunn Høberg-Vetti, Geir Egil Eide, et al.Hereditary Cancer in Clinical Practice|January 11, 2017
How does genetic risk information for Lynch syndrome translate to risk management behaviours?Emma Steel, Andrew Robbins, Mark Jenkins, et al.Hereditary Cancer in Clinical Practice|February 25, 2014
Plasma homocysteine levels and genetic polymorphisms in folate metablism are associated with breast cancer risk in chinese womenXiayu Wu, Tianning Zou, Neng Cao, et al.Hereditary Cancer in Clinical Practice|February 25, 2014
Familial testicular germ cell tumor: no associated syndromic pattern identifiedChristine M Mueller, Larissa A Korde, Mary L McMaster, et al.Hereditary Cancer in Clinical Practice|August 7, 2019
A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau diseaseAnne-Marie Vanbinst, Carola Brussaard, Evelynn Vergauwen, et al.Hereditary Cancer in Clinical Practice|May 22, 2015
A case of squamous cell carcinoma of the skin due to the molecularly confirmed Lynch SyndromeSteven SorscherHereditary Cancer in Clinical Practice|April 16, 2020
A rare missense variant in APC interrupts splicing and causes AFAP in two Danish familiesMalene Djursby, Karin Wadt, Jane Hübertz Frederiksen, et al.Pageof 48