Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences

BACKGROUND: Genetic testing for hereditary cancer syndromes has been revolutionized by next-generation sequencing, which allows for simultaneous review of numerous genes. Multigene panels are regularly offered to patients because of their scope and decreased cost and turnaround time. However, many g...

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Detalles Bibliográficos
Autores principales: Clift, Kristin E., Macklin, Sarah K., Hines, Stephanie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916015/
https://www.ncbi.nlm.nih.gov/pubmed/31890060
http://dx.doi.org/10.1186/s13053-019-0132-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916015/
https://www.ncbi.nlm.nih.gov/pubmed/31890060
http://dx.doi.org/10.1186/s13053-019-0132-6

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