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Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing
Existing guidance regarding clinically informed germline testing for patients with cancer is effective for evaluation of classic hereditary cancer syndromes and established gene/cancer type associations. However, current screening methods may miss patients with rare, reduced penetrance, or otherwise...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421918/ https://www.ncbi.nlm.nih.gov/pubmed/37568048 http://dx.doi.org/10.1038/s41698-023-00429-1 |