Article info
PDFPaper
Law, ethics and medicine
The right not to know and preimplantation genetic diagnosis for Huntington’s disease
- Correspondence to Dr E Asscher, Ethiek en Filosofie van de Geneeskunde, ErasmusMC, Postbus 2040, 3000 CA Rotterdam, The Netherlands; e.asscher{at}erasmusmc.nl
Citation
The right not to know and preimplantation genetic diagnosis for Huntington’s disease
Publication history
- Received May 12, 2009
- Revised September 17, 2009
- Accepted October 5, 2009
- First published December 21, 2009.
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
BMJ Publishing Group Ltd & Institute of Medical Ethics. All rights reserved.
Other content recommended for you
- Britain’s new preimplantation tissue typing policy: an ethical defence
- Extending preimplantation genetic diagnosis: medical and non-medical uses
- Genetic testing and reproductive choice in neurological disorders
- Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?
- Clinical applications of preimplantation genetic testing
- Preimplantation genetic testing
- A brief and personal history of ‘what’s in a name’ in reproductive genetics
- Preimplantation genetic diagnosis in clinical practice
- Three models for the regulation of polygenic scores in reproduction
- An analysis of US fertility centre educational materials suggests that informed consent for preimplantation genetic diagnosis may be inadequate