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3. Genetics test report urges moratorium on disclosure. Gammie F Nature; 1993 Dec; 366(6455):498. PubMed ID: 8255280 [No Abstract] [Full Text] [Related]
4. Genetic screening: a response to Nuffield. Clarke A Bull Med Ethics; 1994 Apr; No. 97():13-21. PubMed ID: 11659804 [No Abstract] [Full Text] [Related]
5. Rethinking medical confidentiality: the impact of genetics. Wachbroit R Suffolk Univ Law Rev; 1993; 27(4):1391-410. PubMed ID: 11657043 [No Abstract] [Full Text] [Related]
6. Mentally ill patients need protection from inappropriate genetic testing. Brooks A BMJ; 1998 Oct; 317(7163):903. PubMed ID: 11645106 [No Abstract] [Full Text] [Related]
8. In defence of ignorance: genetic information and the right not to know. Laurie GT Eur J Health Law; 1999 Jun; 6(2):119-32. PubMed ID: 11657815 [No Abstract] [Full Text] [Related]
10. Ethics of genetic screening: the first report of the Nuffield Council on Bioethics. Gillon R J Med Ethics; 1994 Jun; 20(2):67-8, 92. PubMed ID: 8083874 [No Abstract] [Full Text] [Related]
11. Genetics and insurance in Britain: why more than just the Atlantic divides the English-speaking nations. Wilkie T Nat Genet; 1998 Oct; 20(2):119-21. PubMed ID: 9771702 [TBL] [Abstract][Full Text] [Related]
12. Gene test rules 'lack teeth. Coghlan A New Sci; 1996 Dec; 152(2059):6. PubMed ID: 11656573 [No Abstract] [Full Text] [Related]
13. Autonomy, respect, and genetic information policy: a reply to Tuija Takala and Matti Häyry. Rhodes R J Med Philos; 2000 Feb; 25(1):114-20. PubMed ID: 11645210 [No Abstract] [Full Text] [Related]
14. National Ethical Consultative Committee for the Life and Health Sciences in France issues opinion entitled "Genetics and medicine: from prediction to prevention. Int Dig Health Legis; 1996; 47(2):263-5. PubMed ID: 11655202 [No Abstract] [Full Text] [Related]
15. Patients' rights or family responsibilities? Two approaches to genetic testing. Skene L Med Law Rev; 1998; 6(1):1-41. PubMed ID: 11657222 [No Abstract] [Full Text] [Related]
16. Roundtable: the politics of genetic testing. Charo RA; Cook-Deegan RM; Eisenberg RS; Geller G; Finneran K Issues Sci Technol; 1996; 13(1):48-54. PubMed ID: 11654760 [No Abstract] [Full Text] [Related]
17. Genomic torts: the law of the future -- the duty of physicians to disclose the presence of a genetic disease to the relatives of their patients with the disease. Deftos LJ Univ San Francisco Law Rev; 1997; 32(1):105-37. PubMed ID: 11660530 [No Abstract] [Full Text] [Related]
18. Towards a reconstruction of the "genetic family": new principles? Knoppers BM Int Dig Health Legis; 1998; 49(1):241-53. PubMed ID: 11658002 [No Abstract] [Full Text] [Related]
19. Publication-related risks to privacy: ethical implications of pedigree studies. Powers M IRB; 1993; 15(4):7-11. PubMed ID: 11652150 [No Abstract] [Full Text] [Related]
20. Torts and the double helix: malpractice liability for failure to warn of genetic risks. Andrews LB Houst Law Rev; 1992; 29(1):149-84. PubMed ID: 11656665 [No Abstract] [Full Text] [Related] [Next] [New Search]