Unraveling non‐participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors.
Although genomic research offering next‐generation sequencing (NGS) has increased the diagnoses of rare/ultra‐rare disorders, populations experiencing health disparities infrequently participate in these studies. The factors underlying non‐participation would most reliably be ascertained from indivi...
| Published in: | Journal of Genetic Counseling Vol. 32; no. 5; pp. 993 - 1009 |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
| Format: | research tables/charts Journal Article |
| Published: |
Wiley-Blackwell
Oct2023
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| Online Access: | View this record in EBSCOhost |