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1 Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study [期刊论文]

来源：BMC Medical Genomics , 2023

作者:Amina Scherz;Manuela Rabaglio;Muriel Fluri;等

关键词:Hereditary breast and ovarian cancer;Lynch syndrome;...

使用许可:CC BY

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2 Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer [期刊论文]

来源：Breast care , 2023

作者:Rhiem, Kerstin;Zachariae, Silke;Waha, Anke;等

关键词:BRCA1;BRCA2;...

使用许可:CC BY

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3 Refinement of the assignment to the ACMG/AMP BS3 and PS3 criteria of eight BRCA1 variants of uncertain significance by integrating available functional data with protein interaction assays [期刊论文]

来源：Frontiers in Oncology , 2023

作者:Paolo Radice, Laura Caleca

关键词:hereditary breast/ovarian cancer (HBOC);BRCA1;...

使用许可:Unknown

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4 Genetic testing for hereditary breast cancer in Poland: 1998–2022 [期刊论文]

来源：Hereditary Cancer in Clinical Practice , 2023

作者:Steven A Narod;Anna Jakubowska;Jacek Gronwald;等

关键词:BRCA1;BRCA2;...

使用许可:CC BY

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5 Similarities and differences in gene expression profiles of BRCA1 methylated and mutated epithelial ovarian cancers [期刊论文]

来源：Frontiers in Oncology , 2023

作者:Antonella Cromi;Maria Grazia Tibiletti;Laura Libera;等

关键词:BRCA1;NanoString;...

使用许可:Unknown

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6 Corrigendum: A novel BRCA1 splicing variant detected in an early onset triple-negative breast cancer patient additionally carrying a pathogenic variant in ATM: a case report [期刊论文]

来源：Frontiers in Oncology , 2023

作者:Carmen Molica;Elisa Minenza;Annamaria Mosconi;等

关键词:BRCA1;ATM;...

使用许可:Unknown

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