These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
64. Using clients. Cain P Nurs Ethics; 1997 Nov; 4(6):465-71. PubMed ID: 9416105 [TBL] [Abstract][Full Text] [Related]
65. Pathologists enter debate on consent for genetic research on stored tissue. Stephenson J JAMA; 1996 Feb; 275(7):503-4. PubMed ID: 8606455 [No Abstract] [Full Text] [Related]
66. Trends in ethical and legal frameworks for the use of human biobanks. Cambon-Thomsen A; Rial-Sebbag E; Knoppers BM Eur Respir J; 2007 Aug; 30(2):373-82. PubMed ID: 17666560 [TBL] [Abstract][Full Text] [Related]
67. Ethical issues and molecular biology in urology. Neal DE Br J Urol; 1995 Nov; 76 Suppl 2():65-70. PubMed ID: 8535758 [No Abstract] [Full Text] [Related]
68. Nonconsensual participation in genetic studies. Lippman A Am J Public Health; 1996 Jul; 86(7):1030. PubMed ID: 8669508 [No Abstract] [Full Text] [Related]
69. Identifying people's genes: ethical aspects of DNA sampling in populations. Baird PA Perspect Biol Med; 1995; 38(2):159-66. PubMed ID: 7899053 [No Abstract] [Full Text] [Related]
70. Is respect for autonomy defensible? Wilson J J Med Ethics; 2007 Jun; 33(6):353-6. PubMed ID: 17526687 [TBL] [Abstract][Full Text] [Related]
71. The case against contract: participant and investigator duty in clinical trials. De Ville K Am J Bioeth; 2011 Apr; 11(4):16-8. PubMed ID: 21480066 [No Abstract] [Full Text] [Related]
73. Human genetic databases and liberty. Adalsteinsson R Jurid Rev; 2004; 2004(1):65-74. PubMed ID: 16755701 [TBL] [Abstract][Full Text] [Related]
74. Confidentiality for whom? Robinson I Soc Sci Med; 1991; 32(3):279-86. PubMed ID: 2024137 [TBL] [Abstract][Full Text] [Related]
75. 'Science is really needed--that's all I know': informed consent and the non-verbal practices of collecting blood for genetic research in northern Sweden. Hoeyer K New Genet Soc; 2003 Dec; 22(3):229-44. PubMed ID: 15115024 [TBL] [Abstract][Full Text] [Related]
76. For sale in Iceland: a nation's genetic code. Schwartz J Washington Post; 1999 Jan; ():A1, A4. PubMed ID: 11647691 [No Abstract] [Full Text] [Related]
77. Icelandic health records. Andersen B Science; 1998 Dec; 282(5396):1993. PubMed ID: 9874648 [No Abstract] [Full Text] [Related]
78. ASHG report. Statement on informed consent for genetic research. The American Society of Human Genetics. Am J Hum Genet; 1996 Aug; 59(2):471-4. PubMed ID: 8755936 [No Abstract] [Full Text] [Related]
79. Genetic privacy. Gostin LO J Law Med Ethics; 1995; 23(4):320-30. PubMed ID: 8715052 [No Abstract] [Full Text] [Related]
80. Ethical considerations when conducting ethnographic research in a nursing home setting. Schuster E J Aging Stud; 1996; 10(1):57-67. PubMed ID: 11768415 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]