Solidarity and equity: new ethical frameworks for genetic databases
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[1] R. Chadwick,et al. The Icelandic database—do modern times need modern sagas? , 1999, BMJ.
[2] Y. Christen,et al. Genetic Approaches to Coronary Heart Disease and Hypertension , 1991, Springer Berlin Heidelberg.
[3] G. Poste,et al. Building Population Genetics Resources Using the U.K. NHS , 1999, Science.
[4] S. Hunt,et al. A Population Perspective for Genetics Research and Applications to Control Cardiovascular Disease in Utah , 1991 .
[5] G. Annas,et al. Rules for research on human genetic variation--lessons from Iceland. , 2000, The New England journal of medicine.
[6] Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S) , 1994, The Lancet.
[7] J. Kaye,et al. Safeguards for research using large scale DNA collections , 2000, BMJ : British Medical Journal.
[8] Kári Stefánsson,et al. Protection of privacy by third-party encryption in genetic research in Iceland , 2000, European Journal of Human Genetics.
[9] C. Weijer. Protecting Communities in Research: Philosophical and Pragmatic Challenges , 1999, Cambridge Quarterly of Healthcare Ethics.
[10] T. Hope,et al. Essential Practice in Patient-Centred Care , 1996 .
[11] S. Plattner,et al. National Bioethics Advisory Commission , 2001 .
[12] M. Warnock,et al. Informed consent in medical research. , 1998, BMJ.
[13] K. Stefánsson,et al. The Icelandic Healthcare Database and informed consent. , 2000, The New England journal of medicine.