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48. Ethical implications of the Human Genome Diversity Project. McPherson EC Nursingconnections; 1995; 8(1):36-43. PubMed ID: 7777074 [No Abstract] [Full Text] [Related]
49. Legal and ethical issues in psychiatric genetic research. Shore D; Berg K; Wynne D; Folstein MF Am J Med Genet; 1993 May; 48(1):17-21. PubMed ID: 8357032 [TBL] [Abstract][Full Text] [Related]
50. Ethical and legal considerations for IRBs: research with medical records. Cowan DH; Adams BR IRB; 1979 Dec; 1(8):1-4+. PubMed ID: 11661790 [No Abstract] [Full Text] [Related]
51. Setting standards for DNA banks: toward a model code of conduct. McEwen JE; Reilly PR Microb Comp Genomics; 1996; 1(3):165-77. PubMed ID: 9689211 [TBL] [Abstract][Full Text] [Related]
52. Informed consent and patient's rights documents: a right, a rite, or a rewrite? Hochhauser M Ethics Behav; 1999; 9(1):1-20. PubMed ID: 11657485 [TBL] [Abstract][Full Text] [Related]
53. Ethics briefings: confidentiality; organ donation; insurance; the Icelandic database. English V; Heath L; Romano-Critchley G; Sommerville A J Med Ethics; 2000 Jun; 26(3):215-6. PubMed ID: 11645220 [No Abstract] [Full Text] [Related]
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57. Iceland OKs private health databank. Enserink M Science; 1999 Jan; 283(5398):13. PubMed ID: 9917253 [No Abstract] [Full Text] [Related]
58. Policy forum: health care delivery. Building populations genetics resources using the U.K. NHS. Fears R; Poste G Science; 1999 Apr; 284(5412):267-8. PubMed ID: 10232974 [No Abstract] [Full Text] [Related]
59. Ethical issues involved in establishing a registry for familial Alzheimer's disease. Godard B; Knoppers BM; Glass K; Grenon M; Bouchard R; Bouvier M; Goulet J; Gauvreau D Alzheimer Dis Assoc Disord; 1994; 8(2):79-93. PubMed ID: 8060610 [TBL] [Abstract][Full Text] [Related]