Showing results (21-30 of 1,502) with videos related to
Sort By:
Pageof 151
Familial Cancer|January 17, 2012
Can a gastrointestinal pathologist identify microsatellite instability in colorectal cancer with reproducibility and a high degree of specificity?Eli Brazowski, Paul Rozen, Sara Pel, et al.Familial Cancer|March 8, 2012
Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian familiesMiklós Tanyi, Judit Olasz, Janos L Tanyi, et al.Familial Cancer|February 24, 2012
A prospective study of bowel preparation for colonoscopy with polyethylene glycol-electrolyte solution versus sodium phosphate in Lynch syndrome: a randomized trialMaria W J van Vugt van Pinxteren, Mariëtte C A van Kouwen, Martijn G H van Oijen, et al.Familial Cancer|August 30, 2008
Recurring MLH1 deleterious mutations in unrelated Chinese Lynch syndrome families in SingaporeHui-Ling Yap, Wei-Shieng Chieng, Jasmine Rui-Chen Lim, et al.Familial Cancer|August 30, 2008
Familial nasopharyngeal carcinoma in Hong Kong: epidemiology and implication in screeningWai Tong Ng, Cheuk Wai Choi, Michael C H Lee, et al.Familial Cancer|September 2, 2008
Use of total abdominal hysterectomy and hormone replacement therapy in BRCA1 and BRCA2 mutation carriers undergoing risk-reducing salpingo-oophorectomyC A Gabriel, J Tigges-Cardwell, J Stopfer, et al.Familial Cancer|September 3, 2008
Family history is a significant risk factor for pancreatic cancer: results from a systematic review and meta-analysisJennifer Permuth-Wey, Kathleen M EganFamilial Cancer|October 7, 2021
Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancerKyra Bokkers, Ronald P Zweemer, Marco J Koudijs, et al.Familial Cancer|October 20, 2021
Identification of women at risk of hereditary breast-ovarian cancer among participants in a population-based breast cancer screeningLuigina Bonelli, Ivana Valle, Ivana Rebora, et al.Familial Cancer|June 27, 2019
Multiple primary malignancies associated with a germline SMARCB1 pathogenic variantJudith A Eelloo, Miriam J Smith, Naomi L Bowers, et al.Pageof 151