新規登録 | ログイン | FAQ      [?] 

タグ: recontact [18 articles]

Recent papers classified by the tag recontact.
  • Protecting communities in research: current guidelines and limits of extrapolation.
    Nat Genet, Vol. 23, No. 3. (November 1999), pp. 275-280.
    by C Weijer, G Goldsand, EJ Emanuel
  • The duty to recontact: benefit and harm.
    Am J Hum Genet, Vol. 65, No. 4. (October 1999), pp. 1201-1204.
    by NF Sharpe
  • Genetic testing and human subjects in research.
    Whittier Law Rev, Vol. 24, No. 2. (2002), pp. 429-472.
    by SA Laidlaw, LJ Raffel, JF Daar
  • Disseminating the results of participant-focused research.
    J Transcult Nurs, Vol. 10, No. 4. (October 1999), pp. 340-349.
  • Ethical, legal, and practical concerns about recontacting patients to inform them of new information: the case in medical genetics.
    Am J Med Genet, Vol. 103, No. 4. (1 November 2001), pp. 265-276.
    by AG Hunter, N Sharpe, M Mullen, WS Meschino
  • The duty to recontact: attitudes of genetics service providers.
    Am J Hum Genet, Vol. 64, No. 3. (March 1999), pp. 852-860.
    by JL Fitzpatrick, C Hahn, T Costa, MJ Huggins
  • notes The complex relationship of genetics, groups, and health: what it means for public health.
    J Law Med Ethics, Vol. 30, No. 2. (2002), pp. 290-297.
    by EW Clayton
    posted to public-health recontact by ladygoat on 2005-06-23 18:27:02 as ** along with 1 group CGREL
  • notes Staying informed and recontacting patients about research advances: a study of patient attitudes.
    Am J Hum Genet, Vol. 59, No. 4. (October 1996)
    by M Huggins, C Hahn, T Costa
  • Duty to re-contact.
    Genet Med, Vol. 1, No. 4. (n 1999), pp. 171-172.
  • The duty to recontact: attitudes of genetics service providers.
    Am J Hum Genet, Vol. 61, No. 4. (October 1997)
  • Duty to warn at-risk relatives for genetic disease: Genetic counselors' clinical experience
    American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Vol. 119C, No. 1. (17 December 2002), pp. 27-34.
    by Beth B Dugan, Georgia L Wiesner, Eric T Juengst, Maryann O'Riordan, Anne L Matthews, Nathaniel H Robin
  • Disclosure of genetic information obtained through research.
    Genet Test, Vol. 8, No. 3. (2004), pp. 347-355.
    by KA Quaid, NM Jessup, EM Meslin
  • notes Duty to disclose in medical genetics: a legal perspective.
    Am J Med Genet, Vol. 39, No. 3. (1 June 1991), pp. 347-354.
    by MZ Pelias
  • A model agreement for genetic research in socially identifiable populations.
    Am J Hum Genet, Vol. 63, No. 3. (September 1998), pp. 696-702.
    by MW Foster, D Bernsten, TH Carter
  • On warning families about genetic risk: the ghost of Tarasoff.
    Am J Med, Vol. 109, No. 9. (15 December 2000), pp. 738-739.
    by DP Sulmasy
  • notes Medical Geneticists' duty to warn at-risk relatives for genetic disease.
    Am J Med Genet A, Vol. 120, No. 3. (30 July 2003), pp. 374-380.
    by MJ Falk, RB Dugan, MA O'Riordan, AL Matthews, NH Robin
  • Unexpected findings in identifiable stored blood samples after analysis without consent: moral arguments for and against disclosure.
    Genet Couns, Vol. 13, No. 2. (2002), pp. 115-121.
    by MF Verweij, BC Hamel
  • Privacy and disclosure in medical genetics examined in an ethics of care.
    Bioethics, Vol. 5, No. 3. (July 1991), pp. 212-232.
    by DC Wertz, JC Fletcher
  • 注: このページを引用する時は次のURLでどうぞ: http://www.citeulike.org/tag/recontact

    RIS BibTeX
    CiteULike organises scholarly (or academic) papers or literature and provides bibliographic (which means it makes bibliographies) for universities and higher education establishments. It helps undergraduates and postgraduates. People studying for PhDs or in postdoctoral (postdoc) positions. The service is similar in scope to EndNote or RefWorks or any other reference manager like BibTeX, but it is a social bookmarking service for scientists and humanities researchers.