Abstract
Laboratories offering cell-free DNA (cfDNA) often reserve the right to share prenatal genetic data for research. While it is known that non-pregnant patients can be reluctant to share their genetic data for research, the opinions of pregnant patients are unknown. We asked whether pregnant patients who had previously undergone cfDNA were aware that this genetic data may be shared, and examined whether video education about the Genetic Information Nondiscrimination Act (GINA) affected their attitudes toward data sharing.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
