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ladygoat's recontact [18 articles]

当前文献位于 ladygoat's 文献库 标签分类为 recontact. You can also see everyone's recontact.
  • 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
  • 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
  • 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
  • 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
  • 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
  • Disseminating the results of participant-focused research.
    J Transcult Nurs, Vol. 10, No. 4. (October 1999), pp. 340-349.
  • 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
  • DO GENETIC CLINICS HAVE A LEGAL ETHICAL DUTY TO RECONTACT THEIR PATIENTS WHEN NEW INFORMATION ARISES
    AMERICAN JOURNAL OF HUMAN GENETICS, Vol. 57, No. 4., 1704.
    by Jp Cote, Ml Klimek, Cl Johnson
    posted to recontact by ladygoat on 2005-06-23 17:58:18 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
  • 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
  • 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
  • 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: benefit and harm.
    Am J Hum Genet, Vol. 65, No. 4. (October 1999), pp. 1201-1204.
    by NF Sharpe
  • The duty to recontact: attitudes of genetics service providers.
    Am J Hum Genet, Vol. 61, No. 4. (October 1997)
  • 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
  • Disclosure of genetic information obtained through research.
    Genet Test, Vol. 8, No. 3. (2004), pp. 347-355.
    by KA Quaid, NM Jessup, EM Meslin
  • Duty to re-contact.
    Genet Med, Vol. 1, No. 4. (n 1999), pp. 171-172.
  • 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
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