307 related articles for article (PubMed ID: 15040376)
41. Safeguarding human genetic privacy.
Judicature; 2003; 86(5):224. PubMed ID: 15744895
[No Abstract] [Full Text] [Related]
42. International perspectives on ethics and human genetics.
Wertz DC
Suffolk Univ Law Rev; 1993; 27(4):1411-56. PubMed ID: 11657044
[No Abstract] [Full Text] [Related]
43. Ethical implications of the Human Genome Diversity Project.
McPherson EC
Nursingconnections; 1995; 8(1):36-43. PubMed ID: 7777074
[No Abstract] [Full Text] [Related]
44. A map to a new treasure island: the human genome and the concept of common heritage.
Byk C
J Med Philos; 1998 Jun; 23(3):234-46. PubMed ID: 9736186
[TBL] [Abstract][Full Text] [Related]
45. The ethical and legal implications of genetic screening, counseling, and treatment.
Spring CM
Relig Humanism; 1974; 8(4):177-82. PubMed ID: 11663257
[No Abstract] [Full Text] [Related]
46. Comment on a view favoring ignorance of genetic information: confidentiality, autonomy, beneficence and the right not to know.
Bottis MC
Eur J Health Law; 2000 Jun; 7(2):173-83. PubMed ID: 11789513
[No Abstract] [Full Text] [Related]
47. The limits of state laws to protect genetic information.
Annas GJ
N Engl J Med; 2001 Aug; 345(5):385-8. PubMed ID: 11484711
[No Abstract] [Full Text] [Related]
48. Abortion and international law: the status and possible extension of women's right to privacy.
Michel AE
J Fam Law; 1981-1982; 20(2):241-61. PubMed ID: 11655655
[No Abstract] [Full Text] [Related]
49. International research: ethical imperialism or ethical pluralism?
Macklin R
Account Res; 1999; 7(1):59-83. PubMed ID: 11657563
[No Abstract] [Full Text] [Related]
50. Disclosing genetic research results after death of pediatric patients.
Sexton AC; Metcalfe SA
JAMA; 2008 Oct; 300(14):1693-5. PubMed ID: 18840844
[No Abstract] [Full Text] [Related]
51. Ethical considerations of genetic testing.
Fleming DA
J Clin Ethics; 2002; 13(4):316-23. PubMed ID: 12793324
[No Abstract] [Full Text] [Related]
52. Reservations about women: population policy and reproductive rights.
Abrams P
Cornell Int Law J; 1996; 29(1):1-41. PubMed ID: 11660507
[No Abstract] [Full Text] [Related]
53. Legislating for the new predictive genetics.
Galton DJ; O'Donovan K
Hum Reprod Genet Ethics; 2000; 6(2):39-48. PubMed ID: 12530374
[TBL] [Abstract][Full Text] [Related]
54. Disclosure of Genetic Risk: When Genetic Relatives Are Not Family Members.
Gabriel JL; Jankowski J
Am J Bioeth; 2018 Jul; 18(7):77-79. PubMed ID: 30040558
[No Abstract] [Full Text] [Related]
55. 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]
56. Genetic privacy: from the laboratory to the legislature.
Andrews LB
Genome Res; 1995 Oct; 5(3):209-13. PubMed ID: 8593608
[No Abstract] [Full Text] [Related]
57. Genetic testing in the workplace: ethical, legal, and social implications.
Brandt-Rauf PW; Brandt-Rauf SI
Annu Rev Public Health; 2004; 25():139-53. PubMed ID: 15015916
[TBL] [Abstract][Full Text] [Related]
58. Protecting and promoting privacy in an uncertain world: further defences of ignorance and the right not to know.
Laurie GT
Eur J Health Law; 2000 Jun; 7(2):185-91. PubMed ID: 11789514
[No Abstract] [Full Text] [Related]
59. Informed consent in the genetic age.
Goldworth A
Camb Q Healthc Ethics; 1999; 8(3):393-400. PubMed ID: 10388939
[No Abstract] [Full Text] [Related]
60. Thinking ethically about genetic inheritance: liberal rights, communitarianism and the right to privacy for parents of donor insemination children.
Burr J; Reynolds P
J Med Ethics; 2008 Apr; 34(4):281-4. PubMed ID: 18375682
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
