A common genetic variation in GZMB may associate with cancer risk in patients with Lynch syndrome (original) (raw)

Risk of breast cancer in Lynch syndrome: a systematic review

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Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)

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Journal of Medical Genetics, 2007

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A subset of genetic susceptibility variants for colorectal cancer also has prognostic value

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Molecular Analyses in Diagnosis of High Genetic Predispositions to Malignancies

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2010

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Inherited Genetic Susceptibility to Breast Cancer in Pakistan

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Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome

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Epidemiology and the genetic basis of disease

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Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients with Suspected Lynch Syndrome

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Molecular characteristics of inherited breast tumors

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Meeting abstracts from the Annual Conference on Hereditary Cancers 2015

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The Correlation betweenIL-1β-C31TGene Polymorphism and Susceptibility to Breast Cancer

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S1990 High Cumulative and Relative Cancer Risk and Increased Mortality in Patients With Peutz-Jeghers Syndrome

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The Landscape of Candidate Driver Genes Differs between Male and Female Breast Cancer

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A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns

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Diagnosis of geneticforms of azoospermia

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Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome

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Genetic modifiers of cancer risk in Lynch syndrome: a review

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Quality colonoscopy and risk of interval cancer in Lynch syndrome

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Cancer heterogeneity: origins and implications for genetic association studies

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Lynch syndrome mutations shared by the Baltic States and Poland

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Five Genetic Variants Associated with Prostate Cancer

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New England Journal of Medicine, 2008

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Genome-wide association study of germline variants and breast cancer-specific mortality

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The importance of molecular genetics for cancer screening

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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (vol 22, pg 15, 2020)

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Genetic testing for Usher syndrome

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Genomic medicine and risk prediction across the disease spectrum

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Critical Reviews in Clinical Laboratory Sciences, 2015

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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome

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Gene expression in inherited breast cancer

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Advances in Cancer Research, 2002

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