306 related articles for article (PubMed ID: 15040376)
1. 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]
2. 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]
3. Privacy and disclosure in medical genetics examined in an ethics of care.
Wertz DC; Fletcher JC
Bioethics; 1991 Jul; 5(3):212-32. PubMed ID: 11659340
[TBL] [Abstract][Full Text] [Related]
4. The most personal information of all: an appraisal of genetic privacy in the shadow of the Human Genome Project.
Laurie GT
Int J Law Policy Family; 1996; 10(1):74-101. PubMed ID: 16883663
[TBL] [Abstract][Full Text] [Related]
5. Ethical and juridical issues of genetic testing: a review of the international regulation.
Nicolás P
Crit Rev Oncol Hematol; 2009 Feb; 69(2):98-107. PubMed ID: 19036602
[TBL] [Abstract][Full Text] [Related]
6. MSJAMA. The dilemma of confidentiality in Huntington disease.
Wusthoff C
JAMA; 2003 Sep; 290(9):1219-20. PubMed ID: 12953009
[No Abstract] [Full Text] [Related]
7. The Human Genome Project: a challenge to the human rights framework.
Iles AT
Harv Hum Rights J; 1996; 9():27-60. PubMed ID: 11660498
[No Abstract] [Full Text] [Related]
8. 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]
9. Information(al) matters: bioethics and the boundaries of the public and the private.
Parker LS
Soc Philos Policy; 2002; 19(2):83-112. PubMed ID: 12678083
[No Abstract] [Full Text] [Related]
10. An interest in human dignity as the basis for genomic torts.
Brownsword R
Washburn Law J; 2003; 42(3):413-81. PubMed ID: 15112710
[No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. Property rights in genetic information.
Spinello RA
Ethics Inf Technol; 2004; 6(1):29-42. PubMed ID: 16969959
[TBL] [Abstract][Full Text] [Related]
14. Where in the world are we going with the new genetics?
Fletcher JC
J Contemp Health Law Policy; 1989; 5():33-51. PubMed ID: 11645622
[No Abstract] [Full Text] [Related]
15. Genetic privacy: orthodoxy or oxymoron?
Sommerville A; English V
J Med Ethics; 1999 Apr; 25(2):144-50. PubMed ID: 10226920
[TBL] [Abstract][Full Text] [Related]
16. Privacy of genetic information.
Setoyama K
Osaka Univ Law Rev; 2005 Feb; 52():75-105. PubMed ID: 16482694
[No Abstract] [Full Text] [Related]
17. 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]
18. Genetic testing and insurance: an international comparison.
Simon J
J Int Bioethique; 2003; 14(3-4):59-78. PubMed ID: 15281200
[No Abstract] [Full Text] [Related]
19. Autonomy, informed consent, and genetic testing: an uneasy tension.
Hamilton R; Bowers B
J Nurs Law; 2003 May; 9(1):7-17. PubMed ID: 15282895
[No Abstract] [Full Text] [Related]
20. Genetic privacy: the potential for genetic discrimination in insurance.
Jensen P
Law Rev; 1999 Apr; 29(2):347-69. PubMed ID: 12741371
[No Abstract] [Full Text] [Related]
[Next] [New Search]