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Familial Cancer|September 1, 2006
The 471delAAAG mutation and C353T polymorphism in the RNASEL gene in sporadic and inherited cancer in IsraelEfrat Dagan, Yael Laitman, Nurit Levanon, et al.
Familial Cancer|May 11, 2005
Multiple endocrine neoplasia type 2Mariola Peczkowska, Andrzej Januszewicz
Familial Cancer|May 31, 2007
Sharing experiences of user involvement in shaping new services: the story of a national patient groupAlison Donaldson, Elizabeth Lank, Jane Maher
Familial Cancer|May 18, 2007
The Teesside cancer family history service: change management and innovation at cancer network levelPaul Brennan, Oonagh Claber, Tracey Shaw
Familial Cancer|July 11, 2006
What is the appropriate screening protocol in Lynch syndrome?A E de Jong, F M Nagengast, J H Kleibeuker, et al.
Familial Cancer|July 4, 2006
The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancerBritta Halvarsson, Annika Lindblom, Eva Rambech, et al.
Familial Cancer|July 3, 2021
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone familyKevin M Brown, Mai Xu, Michael Sargen, et al.
Familial Cancer|January 4, 2021
Hereditary medullary thyroid carcinoma syndromes: experience from western IndiaChakra Diwaker, Vijaya Sarathi, Sanjeet Kumar Jaiswal, et al.
Familial Cancer|March 19, 2013
Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutationDongwon Kim, Eunyoung Kang, Euijun Hwang, et al.
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