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Familial Cancer|August 2, 2012
Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairmentLaura Belvederesi, Francesca Bianchi, Cristian Loretelli, et al.
Familial Cancer|August 15, 2012
Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?Philippe Grandval, Emmanuelle Barouk-Simonet, Myriam Bronner, et al.
Familial Cancer|July 26, 2012
Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutationChihiro Kijima, Toshiyuki Miyashita, Maiko Suzuki, et al.
Familial Cancer|June 20, 2012
Outcomes of a systems-level intervention offering breast cancer risk assessments to low-income underserved womenDarren Mays, McKane E Sharff, Tiffani A DeMarco, et al.
Familial Cancer|June 22, 2012
Novel germline c-MET mutation in a family with hereditary papillary renal carcinomaKarin A W Wadt, Anne-Marie Gerdes, Thomas V O Hansen, et al.
Familial Cancer|May 12, 2023
Colonoscopy surveillance in Lynch syndrome is burdensome and frequently delayedElsa L S A van Liere, Imke L Jacobs, Evelien Dekker, et al.
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