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

Journal Abstract Search


277 related items for PubMed ID: 19003717

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

  • 2. What does it mean to be identifiable?
    Hull SC, Wilfond BS.
    Am J Bioeth; 2008 Oct; 8(10):W7-8. PubMed ID: 19003695
    [No Abstract] [Full Text] [Related]

  • 3. Identifiability of DNA data: the need for consistent federal policy.
    McGuire AL.
    Am J Bioeth; 2008 Oct; 8(10):75-6. PubMed ID: 19003718
    [No Abstract] [Full Text] [Related]

  • 4. Ethics as an act of listening.
    Lipworth W, Morrell B, Kerridge I.
    Am J Bioeth; 2008 Oct; 8(10):80-1. PubMed ID: 19003720
    [No Abstract] [Full Text] [Related]

  • 5. Ethics. Identifiability in genomic research.
    Lowrance WW, Collins FS.
    Science; 2007 Aug 03; 317(5838):600-2. PubMed ID: 17673640
    [No Abstract] [Full Text] [Related]

  • 6. Patients' views on identifiability of samples and informed consent for genetic research.
    Hull SC, Sharp RR, Botkin JR, Brown M, Hughes M, Sugarman J, Schwinn D, Sankar P, Bolcic-Jankovic D, Clarridge BR, Wilfond BS.
    Am J Bioeth; 2008 Oct 03; 8(10):62-70. PubMed ID: 19003716
    [Abstract] [Full Text] [Related]

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

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

  • 9. Ethical and legal implications of whole genome and whole exome sequencing in African populations.
    Wright GE, Koornhof PG, Adeyemo AA, Tiffin N.
    BMC Med Ethics; 2013 May 28; 14():21. PubMed ID: 23714101
    [Abstract] [Full Text] [Related]

  • 10. Misusing informed consent: a critique of limitations on research subjects' access to genetic research results.
    Banks TM.
    Sask Law Rev; 2000 May 28; 63(2):539-80. PubMed ID: 12666671
    [Abstract] [Full Text] [Related]

  • 11. Iceland's plan for genomics research: facts and implications.
    Greely HT.
    Jurimetrics; 2000 May 28; 40():153-91. PubMed ID: 16295921
    [Abstract] [Full Text] [Related]

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

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Ethical genetic research on human subjects.
    Harris J.
    Jurimetrics; 1999 May 28; 40():77-91. PubMed ID: 16285118
    [Abstract] [Full Text] [Related]

  • 16. Community participation and representation in genetic studies: testing the application of fundamental ethical principles.
    Brito A.
    St Thomas Law Rev; 2001 May 28; 13(4):935-43. PubMed ID: 12661583
    [No Abstract] [Full Text] [Related]

  • 17. Laboratory specimens and genetic privacy: evolution of legal theory.
    Lewis MH.
    J Law Med Ethics; 2013 Mar 28; 41 Suppl 1():65-8. PubMed ID: 23590744
    [Abstract] [Full Text] [Related]

  • 18. Population-based genetic studies: informed consent and confidentiality.
    Smith MJ.
    Santa Clara Comput High Technol Law J; 2001 Dec 28; 18(1):57-93. PubMed ID: 12741383
    [No Abstract] [Full Text] [Related]

  • 19. Whose genes are they anyway?
    Nelkin D, Andrews LB.
    Chron High Educ; 1999 May 21; 45():B6. PubMed ID: 14598853
    [No Abstract] [Full Text] [Related]

  • 20. Genetic information and the importance of context: implications for the social meaning of genetic information and individual identity.
    Gatter KM.
    St Louis Univ Law J; 2003 May 21; 47(2):423-62. PubMed ID: 15478258
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 14.