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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,...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
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 |
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