Testing the limits of the ‘joint account’ model of genetic information: a legal thought experiment

, &
Journal of Medical Ethics 41 (5):379-382 (2015)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Categories

Keywords

Reprint years

DOI

10.1136/medethics-2014-102142

Other Versions

No versions found

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 99,445

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

My notes

Similar books and articles

Heredity: Science and Society: On the Possibilities and Limits of Genetic Testing and Gene Therapy.Mary J. Seller - 1992 - Journal of Medical Ethics 18 (1):51-51.
From proband to provider: is there an obligation to inform genetic relatives of actionable risks discovered through direct-to-consumer genetic testing?Jordan A. Parsons & Philip E. Baker - 2022 - Journal of Medical Ethics 48 (3):205-212.
An Examination of the Ethical and Legal Limits in Implementing “Traceback Testing” for Deceased Patients.Jessica Martucci, Yolanda Prado, Alan F. Rope, Sheila Weinmann, Larissa White, Jamilyn Zepp, Nora B. Henrikson, Heather Spencer Feigelson, Jessica Ezzell Hunter & Sandra Soo-Jin Lee - 2022 - Journal of Law, Medicine and Ethics 50 (4):818-832.
Should Children and Adolescents Be Tested for Huntington’s Disease? Attitudes of Future Lawyers and Physicians in Switzerland.Bernice S. Elger & Timothy W. Harding - 2006 - Bioethics 20 (3):158-167.
Whole genome sequencing in children: ethics, choice and deliberation.Ainsley J. Newson - 2017 - Journal of Medical Ethics 43 (8):540-542.
Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.Nina Hallowell, Claire Foster, Ros Eeles, A. Ardern-Jones, Veronica Murday & Maggie Watson - 2003 - Journal of Medical Ethics 29 (2):74-79.
Ethical and Legal Challenges Associated with Public Molecular Autopsies.Quianta L. Moore, Mary A. Majumder, Lindsey K. Rutherford & Amy L. McGuire - 2016 - Journal of Law, Medicine and Ethics 44 (2):309-318.
Regulatory and medical aspects of direct-to-consumer genetic testing.M. Sharkey Catherine, Michael Xiaohan Wu & Kenneth Offit F. Walsh - 2021 - In I. Glenn Cohen, Nita A. Farahany, Henry T. Greely & Carmel Shachar (eds.), Consumer genetic technologies: ethical and legal considerations. New York, NY: Cambridge University Press.
Genetics and Life Insurance: Medical Underwriting and Social Policy.Arthur L. Caplan - 2004 - MIT Press.
Drafting the Genetic Privacy Act: Science, Policy, and Practical Considerations.George J. Annas, Leonard H. Glantz & Patricia A. Roche - 1995 - Journal of Law, Medicine and Ethics 23 (4):360-366.

Analytics

Added to PP
2014-06-28

Downloads
49 (#362,804)

6 months
7 (#541,996)

Historical graph of downloads
How can I increase my downloads?

Author's Profile

Citations of this work

Who Counts as Family: A Pluralistic Account of Family in the Genetic Context.Serene Ong - 2022 - International Journal of Feminist Approaches to Bioethics 15 (2):1-21.

Add more citations

References found in this work

Medical law and ethics.Jonathan Herring - 2006 - New York: Oxford University Press.
Please Don’t Tell Me.Jonathan Herring & Charles Foster - 2012 - Cambridge Quarterly of Healthcare Ethics 21 (1):20-29.

Add more references