Article info
PDFGenetics
The routinisation of genomics and genetics: implications for ethical practices
- Correspondence to: Morris W Foster Department of Anthropology, University of Oklahoma, 455 W Lindsey, Rm 505C, Norman, OK 73019, USA; morris.w.foster-1{at}ou.edu
Citation
The routinisation of genomics and genetics: implications for ethical practices
Publication history
- Received July 11, 2005
- Accepted November 21, 2005
- Revised November 3, 2005
- First published October 30, 2006.
Online issue publication
April 27, 2016
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 2006 by the Journal of Medical Ethics
Other content recommended for you
- Genetics and public health—evolution, or revolution?
- Genomic privacy, identity and dignity
- Is genetic information relevantly different from other kinds of non-genetic information in the life insurance context?
- Is there a duty to share genetic information?
- Genetic testing in the acute setting: a round table discussion
- ‘There is a lot of good in knowing, but there is also a lot of downs’: public views on ethical considerations in population genomic screening
- Making the ‘genetic counsellor’ in the UK, 1980–1995
- Why tell asymptomatic children of the risk of an adult-onset disease in the family but not test them for it?
- Exceptional know how? Possible pitfalls of routinising genetic services
- Genetic exceptionalism, revisionism, pluralism and convergence in the ethics of insurance: response to commentators