Monitoring ethical, legal, and social issues in developing population genetic databases
- 1 November 2003
- journal article
- research article
- Published by Elsevier in Genetics in Medicine
- Vol. 5 (6) , 451-457
- https://doi.org/10.1097/01.gim.0000093976.08649.1b
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Assessing the impact of biobanksNature Genetics, 2003
- A vision for the future of genomics researchNature, 2003
- Genebanks: A Comparison of Eight Proposed International Genetic DatabasesPublic Health Genomics, 2003
- Population Databases Boom, From Iceland to the U.S.Science, 2002
- The Icelandic genome debateTrends in Biotechnology, 2001
- The Sequence of the Human GenomeScience, 2001
- The Case for Caution — Being protective of Human Dignity in the Face of Corporate Forces Taking Title to Our DNAJournal of Law, Medicine & Ethics, 2001
- Using the internet to disseminate genetics information for public healthPublished by Oxford University Press (OUP) ,2000
- Rules for Research on Human Genetic Variation — Lessons from IcelandNew England Journal of Medicine, 2000
- The Icelandic Healthcare Database and Informed ConsentNew England Journal of Medicine, 2000