scholarly journals Ade novogermlineMLH1mutation in a Lynch syndrome patient with discordant immunohistochemical and molecular biology test results

2012 ◽  
Vol 18 (39) ◽  
pp. 5635 ◽  
Author(s):  
Fabrice Airaud
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Tanya N. Phung ◽  
Elizabeth Lenkiewicz ◽  
Smriti Malasi ◽  
Amit Sharma ◽  
Karen S. Anderson ◽  
...  

2015 ◽  
pp. hyv172 ◽  
Author(s):  
Hidetaka Eguchi ◽  
Kensuke Kumamoto ◽  
Okihide Suzuki ◽  
Masakazu Kohda ◽  
Yuhki Tada ◽  
...  

2011 ◽  
Vol 105 (3) ◽  
pp. 329-330
Author(s):  
Po-Chuan Chen ◽  
Wen-Chau Chen ◽  
Sheau-Chiou Chao ◽  
Bo-Wen Lin ◽  
Shao-Chieh Lin ◽  
...  

2011 ◽  
Vol 27 (5) ◽  
pp. 681-682 ◽  
Author(s):  
Po-Chuan Chen ◽  
Sheau-Chiou Chao ◽  
Keng-Fu Hsu ◽  
Chung-Ta Lee ◽  
Jenq-Chang Lee

2020 ◽  
Vol 17 (5) ◽  
pp. 373-387
Author(s):  
Anusree Subramonian ◽  
Doug Smith ◽  
Elizabeth Dicks ◽  
Lesa Dawson ◽  
Mark Borgaonkar ◽  
...  

Aim: Lynch Syndrome is associated with a significant risk of colorectal carcinoma (CRC) and other cancers. Universal tumor screening is a strategy to identify high-risk individuals by testing all CRC tumors for molecular features suggestive of Lynch Syndrome. Patient interest in screening and preferences for consent have been underexplored. Methods: A postal survey was administered to CRC patients in a Canadian province. Results: Most patients (81.4%) were willing to have tumors tested if universal tumor screening were available and were willing to discuss test results with family members and healthcare professionals. The majority (62.6%) preferred informed consent be obtained prior to screening. Conclusion: Patients were supportive of universal screening. They expected consent to be obtained, contrary to current practice across Canada and elsewhere.


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