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Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing : a qualitative study
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How do researchers acquire and develop notions of research integrity? : a qualitative study among biomedical researchers in Switzerland
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Model consent clauses for rare disease research
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Dual consent? Donors' and recipients' views about involvement in decision-making on the use of embryos created by gamete donation in research
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Huge variation in obtaining ethical permission for a non-interventional observational study in Europe
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Ghent University Hospital’s protocol regarding the procedure concerning euthanasia and psychological suffering
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An update on the 'empirical turn' in bioethics : analysis of empirical research in nine bioethics journals
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The patient perspective in health care networks
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Standards of practice in empirical bioethics research : towards a consensus
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Pre- and post-testing counseling considerations for the provision of expanded carrier screening : exploration of European geneticists’ views