Investigating the prevalence of pathogenic variants in Saudi Arabian patients with familial cancer using a multigene next generation sequencing panel

Family history is an important factor in determining hereditary cancer risk for many cancer types. The emergence of next-generation sequencing (NGS) has expedited the discovery of many hereditary cancer susceptibility genes and the development of rapid, affordable testing kits. Here, a 30-gene targe...

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Detalles Bibliográficos
Autores principales: AlHarbi, Musa, Mobark, Nahla Ali, AlJabarat, Wael Abdel Rahman, ElBardis, Hadeel, AlSolme, Ebtehal, Hamdan, Abdullah Bany, AlFakeeh, Ali H., AlMushawah, Fatimah, AlHarthi, Fawz, AlSharm, Abdullah A., Balbaid, Ali Abdullah O., AlJohani, Naji, Zhou, Alicia Y., Robinson, Heather A., Alqahtani, Saleh A., Abedalthagafi, Malak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2023
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259259/
https://www.ncbi.nlm.nih.gov/pubmed/37306523
http://dx.doi.org/10.18632/oncotarget.28457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259259/
https://www.ncbi.nlm.nih.gov/pubmed/37306523
http://dx.doi.org/10.18632/oncotarget.28457

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