Pages that link to "Q33767027"

The following pages link to Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry (Q33767027):

Displaying 42 items.

• Combined genetic and nutritional risk models of triple negative breast cancer (Q28243823) (← links)
• Cancer risks for MLH1 and MSH2 mutation carriers (Q30563768) (← links)
• Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases (Q33625221) (← links)
• Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations (Q34160516) (← links)
• Microsatellite instability and ploidy status define three categories with distinctive prognostic impact in endometrioid endometrial cancer (Q34227653) (← links)
• Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins (Q34375540) (← links)
• Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer (Q34481263) (← links)
• An intronic mutation in MLH1 associated with familial colon and breast cancer. (Q34565224) (← links)
• Epithelial ovarian cancer: An overview (Q34708560) (← links)
• Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome). (Q35000837) (← links)
• High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry (Q35085756) (← links)
• Promoter methylation of Wnt antagonistsDKK1andSFRP1is associated with opposing tumor subtypes in two large populations of colorectal cancer patients (Q35117267) (← links)
• Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers (Q35744898) (← links)
• Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study (Q35925149) (← links)
• Frequent mismatch-repair defects link prostate cancer to Lynch syndrome (Q35969934) (← links)
• Mutation deep within an intron of MSH2 causes Lynch syndrome (Q36087551) (← links)
• Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases (Q36245422) (← links)
• Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry (Q36331274) (← links)
• Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome (Q36486798) (← links)
• Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort. (Q36602836) (← links)
• Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome (Q36621452) (← links)
• Risk of breast cancer in Lynch syndrome: a systematic review. (Q36903207) (← links)
• Is breast cancer a part of Lynch syndrome? (Q36924401) (← links)
• A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome (Q37089839) (← links)
• Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer (Q37192664) (← links)
• Phenotype-genotype correlation in familial breast cancer (Q37852615) (← links)
• Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families (Q38410255) (← links)
• The cancer genetics and pathology of male breast cancer (Q38696800) (← links)
• Multigene Panel Testing Provides a New Perspective on Lynch Syndrome (Q38780723) (← links)
• Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts (Q40713486) (← links)
• Lynch Syndrome - is breast cancer a feature? (Q46763385) (← links)
• MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer (Q49970913) (← links)
• Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer (Q51063696) (← links)
• Missed opportunities: Genetic counseling and testing among an ethnically diverse cohort of women with endometrial cancer (Q58630051) (← links)
• Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open? (Q60713341) (← links)
• Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome (Q83172998) (← links)
• Genetic Predisposition to Breast and Ovarian Cancers: How Many and Which Genes to Test? (Q89659606) (← links)
• Investigating the Link between Lynch Syndrome and Breast Cancer (Q91879304) (← links)
• Does breast carcinoma belong to the Lynch syndrome tumor spectrum? - Somatic mutational profiles vs. ovarian and colorectal carcinomas (Q91943718) (← links)
• High prevalence of the MLH1 V384D germline mutation in patients with HER2-positive luminal B breast cancer (Q92266340) (← links)
• Using next-generation sequencing to redefine BRCAness in triple-negative breast cancer (Q92770980) (← links)
• The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability (Q97527458) (← links)