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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

140 related items for PubMed ID: 8808617

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Roundtable: the politics of genetic testing.
    Charo RA, Cook-Deegan RM, Eisenberg RS, Geller G, Finneran K.
    Issues Sci Technol; 1996; 13(1):48-54. PubMed ID: 11654760
    [No Abstract] [Full Text] [Related]

  • 4. Testing for HD in twins.
    Reich E, Zanko A, Heimler A.
    J Genet Couns; 1996 Mar; 5(1):47-51. PubMed ID: 11657408
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. When what we know outstrips what we can do.
    McLean MR.
    Issues Ethics; 1998 Mar; 9(2):6-10. PubMed ID: 11660611
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. In defence of ignorance: genetic information and the right not to know.
    Laurie GT.
    Eur J Health Law; 1999 Jun; 6(2):119-32. PubMed ID: 11657815
    [No Abstract] [Full Text] [Related]

  • 14. Genetics is a family affair.
    Webb J.
    New Sci; 1993 Dec 11; 140(1903):9. PubMed ID: 11656285
    [No Abstract] [Full Text] [Related]

  • 15. Privacy and disclosure in medical genetics examined in an ethics of care.
    Wertz DC, Fletcher JC.
    Bioethics; 1991 Jul 11; 5(3):212-32. PubMed ID: 11659340
    [Abstract] [Full Text] [Related]

  • 16. Ethical considerations in the social context of Huntington disease.
    Turner D.
    Dis Markers; 1992 Jul 11; 10(4):171-83; discussion 211-28. PubMed ID: 1304435
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Dilemmas of anonymous predictive testing for Huntington disease: privacy vs. optimal care.
    Burgess MM, Adam S, Bloch M, Hayden MR.
    Am J Med Genet; 1997 Aug 08; 71(2):197-201. PubMed ID: 9217222
    [Abstract] [Full Text] [Related]

  • 20. The family covenant: a flawed response to the dilemmas of genetic testing.
    Stock G.
    Am J Bioeth; 2001 Aug 08; 1(3):17-8. PubMed ID: 11954578
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.