Pages that link to "Q50752107"

The following pages link to High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes. (Q50752107):

Displaying 35 items.

• A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly (Q24633479) (← links)
• Mitogenomic and microsatellite variation in descendants of the founder population of Newfoundland: high genetic diversity in an historically isolated population (Q28305528) (← links)
• Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. (Q30497402) (← links)
• Evaluation of a population-based approach to familial colorectal cancer (Q33628619) (← links)
• Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer (Q33725467) (← links)
• Characterisation of familial colorectal cancer Type X, Lynch syndrome, and non-familial colorectal cancer (Q33994353) (← links)
• Efficacy of an educational intervention on family physicians' risk assessment and management of colorectal cancer (Q34156897) (← links)
• A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expression (Q34239761) (← links)
• Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada. (Q34312480) (← links)
• Serotonin transporter gene (SLC6A4) variations are associated with poor survival in colorectal cancer patients (Q34387391) (← links)
• Colorectal Cancer Incidence Rates in the Louisiana Acadian Parishes Demonstrated to be Among the Highest in the United States (Q34446415) (← links)
• The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease (Q34618184) (← links)
• Functional analysis in mouse embryonic stem cells reveals wild-type activity for three MSH6 variants found in suspected Lynch syndrome patients (Q34990339) (← links)
• Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients (Q35034717) (← links)
• Promoter methylation of Wnt antagonistsDKK1andSFRP1is associated with opposing tumor subtypes in two large populations of colorectal cancer patients (Q35117267) (← links)
• A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer (Q35647279) (← links)
• Promoter methylation of ITF2, but not APC, is associated with microsatellite instability in two populations of colorectal cancer patients. (Q35925613) (← links)
• CoDP: predicting the impact of unclassified genetic variants in MSH6 by the combination of different properties of the protein. (Q36835342) (← links)
• Public attitudes towards genomic risk profiling as a component of routine population screening (Q36957475) (← links)
• Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario (Q37348461) (← links)
• Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis. (Q37400731) (← links)
• Mismatch repair deficiency screening via immunohistochemical staining in young Asians with colorectal cancers (Q38124242) (← links)
• The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome (Q44511151) (← links)
• Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment (Q47317424) (← links)
• Tobacco smoking and colorectal cancer: a population-based case-control study in Newfoundland and Labrador. (Q48777216) (← links)
• Association of rs2282679 A>C polymorphism in vitamin D binding protein gene with colorectal cancer risk and survival: effect modification by dietary vitamin D intake (Q49871641) (← links)
• MSH2 118T>C and MSH6 159C>T promoter polymorphisms and the risk of colorectal cancer (Q50661115) (← links)
• Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies (Q50711835) (← links)
• Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation-positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries. (Q51552333) (← links)
• A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants. (Q54338096) (← links)
• Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. (Q55264458) (← links)
• A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome (Q57735499) (← links)
• Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancer (Q57737908) (← links)
• Evidence for GALNT12 as a moderate penetrance gene for colorectal cancer (Q88635627) (← links)
• Familial Intracranial Aneurysm in Newfoundland: Clinical and Genetic Analysis (Q92481088) (← links)