Low frequency of structured documentation for cancer genetic testing in a large electronic health record dataset: A brief report using All of Us Research data.
Annually, over two million individuals in the United States are diagnosed with cancer, with 10–20% attributed to hereditary cancer syndromes. Genetic testing for pathogenic variants is a standard component of cancer care guided by tumor pathology and family history. Despite this, access to and compl...
| Publicado en: | Journal of Genetic Counseling Vol. 34; no. 2; pp. 1 - 8 |
|---|---|
| Autores principales: | , , , |
| Formato: | research tables/charts Journal Article |
| Publicado: |
Wiley-Blackwell
Apr2025
|
| Acceso en línea: | Ver este registro en EBSCOhost |