Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study
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Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal storiesEthical aspects of registry-based research in the Nordic countriesStakeholders' perspectives on biobank-based genomic research: systematic review of the literaturePublics and biobanks: Pan-European diversity and the challenge of responsible innovationConsent for the use of human biological samples for biomedical research: a mixed methods study exploring the UK public's preferences.Saudi views on consenting for research on medical records and leftover tissue samples.Ethical aspects of human biobanks: a systematic review.Constructing populations in biobanking.Public support and consent preference for biomedical research and biobanking in JordanPatients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.Public opinion about the importance of privacy in biobank research.The ethics of research biobanking: a critical review of the literature.Informed consent, biobank research, and locality: perceptions of breast cancer patients in three European countries.Attitudes and willingness to donate biological samples for research among potential donors in the Italian Twin Register.Public attitudes to the storage of blood left over from routine general practice tests and its use in research.Attitudes of the general public towards the disclosure of individual research results and incidental findings from biobank genomic research in Australia.Biobanking in Israel 2016-17; expressed perceptions versus real life enrollment.An Australian approach to the policy translation of deliberated citizen perspectives on biobanking.Patterns of self-management practices undertaken by cancer survivors: variations in demographic factors.Withdrawal from biobank research: considerations and the way forward.Patients' attitudes to informed consent for genomic research with donated samples.Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns
P2860
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P2860
Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study
description
im Januar 2007 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2007
@uk
name
Perceptions of potential donor ...... anks: a population-based study
@en
Perceptions of potential donor ...... anks: a population-based study
@nl
type
label
Perceptions of potential donor ...... anks: a population-based study
@en
Perceptions of potential donor ...... anks: a population-based study
@nl
prefLabel
Perceptions of potential donor ...... anks: a population-based study
@en
Perceptions of potential donor ...... anks: a population-based study
@nl
P2093
P2860
P1476
Perceptions of potential donor ...... anks: a population-based study
@en
P2093
Asa Kettis-Lindblad
Eva Viberth
Mats G Hansson
P2860
P304
P356
10.1080/14034940600868572
P407
P577
2007-01-01T00:00:00Z