24 results on '"Jenkins, Mark"'
Search Results
2. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
3. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer
4. Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
5. Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation?
6. Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
7. Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline
8. Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas
9. Determining the familial risk distribution of colorectal cancer: a data mining approach
10. Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene
11. Childhood cancers in families with and without Lynch syndrome
12. High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
13. Fertility and apparent genetic anticipation in Lynch syndrome
14. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer
15. Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?
16. Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis
17. Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
18. Mutation deep within an intron of MSH2 causes Lynch syndrome
19. Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis
20. Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis
21. Determining the familial risk distribution of colorectal cancer: a data mining approach
22. Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas.
23. Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
24. Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.