GermlineBRCA1 andHMLH1 mutations in a family with male and female breast carcinoma
Author:
Publisher
Wiley
Subject
Cancer Research,Oncology
Reference22 articles.
1. Clues to the Pathogenesis of Familial Colorectal Cancer
2. Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
3. Tumour spectrum in hereditary non-polyposis colorectal cancer (HNPCC) and in families with “suspected hnpcc”. A population-based study in northern Italy
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1. A Japanese case of ovarian mucinous adenocarcinoma with germline double variants of MSH2 and BRCA2;Journal of Human Genetics;2023-07-07
2. Concurrent Germline BRCA1/2 and Mismatch Repair Mutations in Young-Onset Pancreatic and Colorectal Cancer: The Importance of Comprehensive Germline and Somatic Characterization to Inform Therapeutic Options;JCO Precision Oncology;2022-06
3. Double heterozygotes of BRCA1/BRCA2 and mismatch repair gene pathogenic variants: case series and clinical implications;Breast Cancer Research and Treatment;2021-06-04
4. The implications of BRCA loss of heterozygosity (LOH) and deficient mismatch repair gene (dMMR) expression in the breast cancer of a patient with both inherited breast and ovarian cancer syndrome (BRCA2) and Lynch syndrome (MLH1);Breast Cancer Research and Treatment;2020-02-10
5. Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer;Familial Cancer;2018-05-21
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