Genomic Secondary Findings
Secondary findings are genomic variants unrelated to the original reason for testing but may indicate hereditary health risks. The protocol uses secondary findings to refer to both secondary and incidental findings unless a specific analys…
1 sources - 5 claims
Secondary findings are genomic variants unrelated to the original reason for testing but may indicate hereditary health risks. The protocol uses secondary findings to refer to both secondary and incidental findings unless a specific analysis separates them. The study focuses especially on pediatric settings because evidence and management guidance are limited there.