Citation Tools
PDFGenetics
Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study
Download to a citation manager
Download the citation for this article by clicking on one of the following citation managers:
- Cite this article as:
- Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study
Other content recommended for you
- An investigation of patients’ motivations for their participation in genetics-related research
- Ethical aspects of research into Alzheimer disease. A European Delphi Study focused on genetic and non-genetic research
- What does ‘respect for persons’ require? Attitudes and reported practices of genetics researchers in informing research participants about research
- Cohort profile: the Australian genetics of depression study
- Collecting genetic samples and linked mental health data from adolescents in schools: protocol coproduction and a mixed-methods pilot of feasibility and acceptability
- Healthcare professionals’ and researchers’ understanding of cancer genetics activities: a qualitative interview study
- Pathogenic variants in the healthy elderly: unique ethical and practical challenges
- Achieving online consent to participation in large-scale gene-environment studies: a tangible destination
- Informed consent, participation in, and withdrawal from a population based cohort study involving genetic analysis
- Ethics of genetic testing and research in sport: a position statement from the Australian Institute of Sport