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Exon splicing analysis of intronic variants in multigene cancer panel testing for hereditary breast/ovarian cancer
The use of multigene panel testing for patients with a predisposition to breast/ovarian cancer is increasing as the identification of variants is useful for diagnosis and disease management. We identified pathogenic and likely pathogenic (P/LP) variants of high‐and moderate‐risk genes using a 23‐gen...
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| 出版年: | Cancer Sci |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7540976/ https://ncbi.nlm.nih.gov/pubmed/32761968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cas.14600 |
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