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Examining Gaps in Institutional Policies for Clinical Genomic Data Sharing: A Cross-Jurisdictional Study

2026-03-10

Abstract excerpt

<h4>Background</h4> The sharing of data generated through the course of clinical genetic and genomic testing without explicit patient consent is increasingly important for timely diagnosis and treatment. While many jurisdictions permit the sharing of identifiable data for direct patient care, institutional policies vary in how clearly they specify key elements. When do policies permit sharing of data without expl...

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Literature Corpus work
71fb53c1-6d05-5574-a33b-716c41f3cb04
DOI
10.64898/2026.03.09.26347975
Open publication

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