What can we learn from more than 1,000 Brazilian patients at risk of hereditary cancer?

BACKGROUND: Identifying individuals at a higher risk of developing cancer is a major concern for healthcare providers. Cancer predisposition syndromes are the underlying cause of cancer aggregation and young-onset tumors in many families. Germline genetic testing is underused due to lack of access,...

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Detalles Bibliográficos
Autores principales: Leite, Ana Carolina Rathsam, Suzuki, Daniele Assad, Pereira, Allan Anderson Lima, Machado, Natalia Polidorio, Barroso-Sousa, Romualdo, Correa, Tatiana Strava, Moura, Fernanda Cesar, Morbeck, Igor Alexandre Protzner, Gumz, Brenda Pires, Faria, Luiza Dib Batista Bugiato, Fernandes, Gustavo dos Santos, Sandoval, Renata Lazari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484549/
https://www.ncbi.nlm.nih.gov/pubmed/36132150
http://dx.doi.org/10.3389/fonc.2022.963910

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484549/
https://www.ncbi.nlm.nih.gov/pubmed/36132150
http://dx.doi.org/10.3389/fonc.2022.963910

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