Article info
PDFLaw, ethics and medicine
The right not to know: an autonomy based approach
- Correspondence to: R Andorno Interdepartmental Center for Ethnics in the Sciences and Humanities (IZEW), University of Tübingen, Wilhelmstr. 19, 72074 Tübingen, Germany; roberto.andornouni-tuebingen.de
Citation
The right not to know: an autonomy based approach
Publication history
- Received September 2, 2002
- Accepted July 2, 2003
- Revised May 3, 2003
- First published October 5, 2004.
Online issue publication
October 05, 2004
Author Affiliation
Please note that there is a spelling error in the author affiliation, the correct address details are shown here:
Interdepartmental Center for Ethics in the Sciences and Humanities (IZEW)
University of T�bingen
Wilhelmstr. 19
72074 T�bingen
GermanyThe error is much regretted.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2004 by the Journal of Medical Ethics
Other content recommended for you
- The new genetics: Genetic testing and public policy
- Clinical applications of preimplantation genetic testing
- Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information
- Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?
- From proband to provider: is there an obligation to inform genetic relatives of actionable risks discovered through direct-to-consumer genetic testing?
- Genetic counselling in ALS: facts, uncertainties and clinical suggestions
- Genetic discrimination in life insurance: empirical evidence from a cross sectional survey of genetic support groups in the United Kingdom
- Genetics and public health—evolution, or revolution?
- Perceptions of genetic discrimination among people at risk for Huntington’s disease: a cross sectional survey
- An evaluation of needs of female BRCA1and BRCA2 carriers undergoing genetic counselling