Article info
PDFGenetics
Minors and informed consent in carrier testing: a survey of European clinical geneticists
- P Borry, Kapucijnenvoer 35, Box 7001, 3000 Leuven, Belgium; Pascal.Borry{at}med.kuleuven.be
Citation
Minors and informed consent in carrier testing: a survey of European clinical geneticists
Publication history
- Received May 29, 2007
- Revised July 31, 2007
- Accepted August 2, 2007
- First published April 30, 2008.
Online issue publication
April 30, 2008
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
2008 BMJ Publishing Group & Institute of Medical Ethics
Other content recommended for you
- Inappropriate genetic testing of children
- Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation
- Challenges of genetic testing in adolescents with cardiac arrhythmia syndromes
- Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases
- Implications of carrier identification in newborn screening for cystic fibrosis
- When to break the news and whose responsibility is it? A cross-sectional qualitative study of health professionals’ views regarding disclosure of BRCA genetic cancer risk
- How should health policy and practice respond to the increased genetic risk associated with close relative marriage? results of a UK Delphi consensus building exercise
- Why patients do not attend for their appointments at a genetics clinic
- Guidelines for a genetic risk based approach to advising women with a family history of breast cancer
- The return of individual research findings in paediatric genetic research