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3. Whose genes are they anyway? Nelkin D; Andrews LB Chron High Educ; 1999 May; 45():B6. PubMed ID: 14598853 [No Abstract] [Full Text] [Related]
4. Selected legal and ethical issues relevant to pediatric genetics. Nelson E; Haymond K; Sidarous M Health Law J; 1998; 6 Spec No():83-113. PubMed ID: 14746062 [No Abstract] [Full Text] [Related]
5. Genetic testing without consent: the implications of the new Human Tissue Act 2004. Lucassen A; Kaye J J Med Ethics; 2006 Dec; 32(12):690-2. PubMed ID: 17145906 [TBL] [Abstract][Full Text] [Related]
6. Genetic secrets and the family. Bell D; Bennett B Med Law Rev; 2001; 9(2):130-61. PubMed ID: 12778930 [No Abstract] [Full Text] [Related]
7. Genetic secrets and the family: a response to Bell and Bennett. Skene L Med Law Rev; 2001; 9(2):162-9. PubMed ID: 12778931 [No Abstract] [Full Text] [Related]
8. The new world of genomic testing, families and privacy. Wolf SM Minn Med; 2015 Jun; 98(6):32-4. PubMed ID: 26168658 [No Abstract] [Full Text] [Related]
9. The Genetic Non-Discrimination Act: critical for promoting health and science in Canada. Bombard Y; Heim-Myers B CMAJ; 2018 May; 190(19):E579-E580. PubMed ID: 29759963 [No Abstract] [Full Text] [Related]
10. Can I access my personal genome? The current legal position in the UK. Kaye J; Kanellopoulou N; Hawkins N; Gowans H; Curren L; Melham K Med Law Rev; 2014; 22(1):64-86. PubMed ID: 24136352 [TBL] [Abstract][Full Text] [Related]
11. Relationships matter: ethical considerations for returning results to family members of deceased subjects. Milner LC; Liu EY; Garrison NA Am J Bioeth; 2013; 13(10):66-7. PubMed ID: 24024819 [No Abstract] [Full Text] [Related]
13. Should researchers disclose results to descendants? Rothstein MA Am J Bioeth; 2013; 13(10):64-5. PubMed ID: 24024818 [No Abstract] [Full Text] [Related]
14. Disclosure of genetic tests for health insurance: is it ethical not to? Raithatha N; Smith RD Lancet; 2004 Jan; 363(9406):395-6. PubMed ID: 15070572 [No Abstract] [Full Text] [Related]
15. Misusing informed consent: a critique of limitations on research subjects' access to genetic research results. Banks TM Sask Law Rev; 2000; 63(2):539-80. PubMed ID: 12666671 [TBL] [Abstract][Full Text] [Related]
16. Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility. Cassa CA; Savage SK; Taylor PL; Green RC; McGuire AL; Mandl KD Genome Res; 2012 Mar; 22(3):421-8. PubMed ID: 22147367 [TBL] [Abstract][Full Text] [Related]
17. Pathogenic variants in the healthy elderly: unique ethical and practical challenges. Lacaze P; Ryan J; Woods R; Winship I; McNeil J J Med Ethics; 2017 Oct; 43(10):714-722. PubMed ID: 28341755 [TBL] [Abstract][Full Text] [Related]
18. Genetics and patients' rights: where are the limits? Laurie GT Med Law Int; 2000; 5(1):25-44. PubMed ID: 15040376 [No Abstract] [Full Text] [Related]
19. Genetic testing and human subjects in research. Laidlaw SA; Raffel LJ; Daar JF Whittier Law Rev; 2002; 24(2):429-72. PubMed ID: 15085855 [No Abstract] [Full Text] [Related]
20. PGTandMe: social networking-based genetic testing and the evolving research model. Koch VG Health Matrix Clevel; 2012; 22(1):33-74. PubMed ID: 22616542 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]