Comprehensive analysis of germline mutations in northern Brazil: a panel of 16 genes for hereditary cancer-predisposing syndrome investigation

BACKGROUND: Next generation sequencing (NGS) has been a handy tool in clinical practice, mainly due to its efficiency and cost-effectiveness. It has been widely used in genetic diagnosis of several inherited diseases, and, in clinical oncology, it may enhance the discovery of new susceptibility gene...

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Detalles Bibliográficos
Autores principales: Vidal, Amanda Ferreira, Ferraz, Rafaella Sousa, El-Husny, Antonette, Silva, Caio Santos, Vinasco-Sandoval, Tatiana, Magalhães, Leandro, Raiol-Moraes, Milene, Barra, Williams Fernandes, Pereira, Cynthia Lara Brito Lins, de Assumpção, Paulo Pimentel, de Brito, Leonardo Miranda, Vialle, Ricardo Assunção, Santos, Sidney, Ribeiro-dos-Santos, Ândrea, Ribeiro-dos-Santos, André M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028728/
https://www.ncbi.nlm.nih.gov/pubmed/33827469
http://dx.doi.org/10.1186/s12885-021-08089-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028728/
https://www.ncbi.nlm.nih.gov/pubmed/33827469
http://dx.doi.org/10.1186/s12885-021-08089-9

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