The governance of genetic information who decides? /
Wedi'i Gadw mewn:
| Awdur Corfforaethol: | |
|---|---|
| Awduron Eraill: | , |
| Fformat: | Electronig eLyfr |
| Iaith: | Saesneg |
| Cyhoeddwyd: |
Cambridge ; New York :
Cambridge University Press,
2009.
|
| Cyfres: | Cambridge law, medicine, and ethics.
|
| Pynciau: | |
| Mynediad Ar-lein: | An electronic book accessible through the World Wide Web; click to view |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|
Eitemau Tebyg: The governance of genetic information
- An immense new power to heal the promise of personalized medicine /
- To test or not to test a guide to genetic screening and risk /
- Heredity and hope the case for genetic screening /
- Direct-to-consumer genetic testing summary of a workshop /
- Ethical issues of human genetic databases a challenge to classical health research ethics? /
- DNA promise and peril /