Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers (original) (raw)

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Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

Mary Beattie

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Prevalence of BRCA1 and BRCA2 gene mutations in families with medium and high risk of breast and ovarian cancer in Brazil

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BRCA1 germline mutations may be associated with reduced ovarian reserve

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Case report of a rare variant of BRCA2 germline mutation in an ovarian cancer patient

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Potential Excess Mortality in BRCA1/2 Mutation Carriers beyond Breast, Ovarian, Prostate, and Pancreatic Cancers, and Melanoma

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BRCA immunohistochemistry for screening of BRCA mutation in epithelial ovarian cancer patients

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Founder BRCA1 mutations and two novel germline BRCA2 mutations in breast and/or ovarian cancer families from North-Eastern Poland

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Modern Approaches and Future Perspectives on Breast and Ovarian Cancer Prevention Strategies in BRCA1 and BRCA2 Mutation Carriers: A Literature Overview

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The use of cytogenetics in understanding ovarian cancer

Jeremy A . Squire

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DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas

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BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

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Frequency of three BRCA1 gene founder mutations in breast/ovarian cancer families from the Pomerania-Kujawy region of Poland

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Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases

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Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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High-grade serous ovarian carcinoma and detection of inactivated BRCA genes from biopsy material of Slovak patients

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A new mutation of BRCA2 gene in an Italian healthy woman with familial breast cancer history

Maria Maddalena Galante

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Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients

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Integrated genomic analyses of ovarian carcinoma

William Chang

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Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 Flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease

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Prevalence of germline variants in consensus moderate-to-high-risk predisposition genes to hereditary breast and ovarian cancer in BRCA1/2-negative Brazilian patients

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Integrated analysis of germline and somatic variants in ovarian cancer

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Predisposition testing for breast and ovarian cancer susceptibility

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BRCA1 and BRCA2mutations in breast cancer patients from Venezuela

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Clinicopathological characteristics and BRCA1/BRCA2 pathogenic variants of patients with breast cancer

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Clinical practice guidelines for BRCA1 and BRCA2 genetic testing

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