BLOOD & DATA: ETHICAL, LEGAL AND SOCIAL ASPECTS OF HUMAN GENETIC DATABASES
Reykjavík: University of Iceland Press [and] Centre for Ethics, 2004. 352 p.
Blood; Databases; Genetic Databases; Bioethics; Value / Quality of Life; Social Control of Science and Technology; Sociology of Health Care; Confidentiality; Genetics, Molecular Biology and Microbiology; Genetic Screening / Genetic Testing; Eugenics; Genome Mapping; Genetics and Human Ancestry; Donation / Procurement of Organs and Tissues; International and Political Dimensions of Biology and Medicine; Information Science Ethics; Government Ethics; Research on Special Populations; Economics of Health Care;
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Genetic Testing is Different [reviews of GENETIC TESTING FOR ALZHEIMER DISEASE: ETHICAL AND CLINICAL ISSUES, by Stephen G. Post and Peter J. Whitehouse and PROMOTING SAFE AND EFFECTIVE GENETIC TESTING IN THE UNITED STATES: PRINCIPLES AND RECOMMENDATIONS, by Task Force on Genetic Testing, NIH-DOE Working Group on Ethical, Legal, and Social Implications of Human Genome Research] Clayton, Ellen Wright (2001-04)