An Accessible Communication System for Population-Based Genetic Testing: Development and Usability Study

BACKGROUND: Genetic testing uptake is low, despite the well-established connection between pathogenic variants in certain cancer-linked susceptibility genes and ovarian cancer risk. Given that most major insurers cover genetic testing for those with a family history suggestive of hereditary cancer,...

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Detalles Bibliográficos
Autores principales: Coffin, Tara, Bowen, Deborah, Swisher, Elizabeth, Lu, Karen, Rayes, Nadine, Norquist, Barbara, Blank, Stephanie, Levine, Douglas, Bakkum-Gamez, Jamie, Fleming, Gini, Olopade, Olufunmilayo, D’Andrea, Alan, Nebgen, Denise, Peterson, Christine, Munsell, Mark, Gavin, Kathleen, Lechner, Rebecca, Crase, Jamie, Polinsky, Deborah, Romero, Iris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2022
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623457/
https://www.ncbi.nlm.nih.gov/pubmed/36251350
http://dx.doi.org/10.2196/34055

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623457/
https://www.ncbi.nlm.nih.gov/pubmed/36251350
http://dx.doi.org/10.2196/34055

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