Article info
Law, ethics and medicine
Paper
Biobanks for non-clinical purposes and the new law on forensic biobanks: does the Italian context protect the rights of minors?
- Correspondence to Dr Pamela Tozzo, Department of Environmental Medicine and Public Health, Legal Medicine Unit, University of Padua, Via Falloppio 50, 35121, Padua, Italy; pamela.tozzo{at}unipd.it
Citation
Biobanks for non-clinical purposes and the new law on forensic biobanks: does the Italian context protect the rights of minors?
Publication history
- Received May 5, 2010
- Revised June 30, 2010
- Accepted July 8, 2010
- First published November 8, 2010.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
- You are viewing the most recent version of this article.
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
© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
Other content recommended for you
- Public participation in genetic databases: crossing the boundaries between biobanks and forensic DNA databases through the principle of solidarity
- Forensic DNA databases: genetic testing as a societal choice
- The case of biobank with the law: between a legal and scientific fiction
- Spanish public awareness regarding DNA profile databases in forensic genetics: what type of DNA profiles should be included?
- Commercial DNA tests and police investigations: a broad bioethical perspective
- Accessing medical biobanks to solve crimes: ethical considerations
- Informed consent for the study of retained tissues from postmortem examination following sudden infant death
- The retention of forensic DNA samples: a socio-ethical evaluation of current practices in the EU
- Ethics in studies on children and environmental health
- Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents