Adaptation and early implementation of the PREdiction model for gene mutations (PREMM(5)™) for lynch syndrome risk assessment in a diverse population

Lynch syndrome (LS) is the most common inherited cause of colorectal and endometrial cancers. Identifying individuals at risk for LS without personal cancer history requires detailed collection and assessment of family health history. However, barriers exist to family health history collection, espe...

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Detalles Bibliográficos
Autores principales: Mittendorf, Kathleen F., Ukaegbu, Chinedu, Gilmore, Marian J., Lindberg, Nangel M., Kauffman, Tia L., Eubanks, Donna J., Shuster, Elizabeth, Allen, Jake, McMullen, Carmit, Feigelson, Heather Spencer, Anderson, Katherine P., Leo, Michael C., Hunter, Jessica Ezzell, Sasaki, Sonia Okuyama, Zepp, Jamilyn M., Syngal, Sapna, Wilfond, Benjamin S., Goddard, Katrina A. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458476/
https://www.ncbi.nlm.nih.gov/pubmed/33754278
http://dx.doi.org/10.1007/s10689-021-00243-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458476/
https://www.ncbi.nlm.nih.gov/pubmed/33754278
http://dx.doi.org/10.1007/s10689-021-00243-3

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