Listen to ONS Genomics Advisory Board member, Suzanne Mahon, RN, DNSc, AOCN, AGN-BC as she explains the Genetic Information Nondiscrimination Act (GINA). This information is crucial in supporting your patient that has questions about what happens to their genetic information once you collect it.
Focused content to elevate your practice at the point of care, including toolkits, quick guides, discussion tools, checklists, and clinical updates.
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