Abstract
This article examines ethical issues debated in Iceland concerning population genetic research, specifically methods of collecting biosamples and ways to return clinically relevant results to participants. Also discussed are scientific research in the health sector, a bill on surrogacy, and a policy on consent for organ donation.
| Original language | English |
|---|---|
| Pages (from-to) | 421-434 |
| Number of pages | 14 |
| Journal | Cambridge Quarterly of Healthcare Ethics |
| Volume | 25 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 1 Jul 2016 |
Bibliographical note
Publisher Copyright:© Cambridge University Press 2016.
Other keywords
- Biosamples
- Consent for organ donation
- Population genetic research
- Surrogacy