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Familial Cancer|August 4, 2010
A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese HanHong Guo, Kai Wang, Gang Xiong, et al.Familial Cancer|December 8, 2010
Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis reportMatjaz Vogelsang, Radovan KomelFamilial Cancer|September 30, 2010
A new mutation of BRCA2 gene in an Italian healthy woman with familial breast cancer historyMaurizio Pisanò, Valeria Mezzolla, Maria Maddalena Galante, et al.Familial Cancer|September 30, 2010
An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutationsPaboda Ratnayake, Claire E Wakefield, Bettina Meiser, et al.Familial Cancer|August 28, 2010
Real world experience with cancer genetic counseling via telephoneRebecca Sutphen, Barbara Davila, Heather Shappell, et al.Familial Cancer|September 21, 2010
What I wish I'd known before surgery: BRCA carriers' perspectives after bilateral salipingo-oophorectomyDanielle Campfield Bonadies, Anne Moyer, Ellen T MatloffFamilial Cancer|November 25, 2010
The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancerNing Li, Kang Shao, Zhaoli Chen, et al.Familial Cancer|September 3, 2010
BRCA1 and BRCA2 families and the risk of skin cancerOphira M Ginsburg, Charmaine Kim-Sing, William D Foulkes, et al.Familial Cancer|September 22, 2010
Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch SyndromeKatja I Aktan-Collan, Helena A Kääriäinen, Eeva M Kolttola, et al.Familial Cancer|November 30, 2010
IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancerMaria Henningson, Maria Hietala, Therese Törngren, et al.Pageof 151