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  1. Jürgen Robienski & Jürgen Simon (2010). Pt. 4. Genetics and Health Care Rights. Recent Developments in the Legal Discourse on Genetic Testing in Germany. In André den Exter (ed.), Human Rights and Biomedicine. Maklu.
  2. Jürgen Simon & Cristina Blohm-Seewald (2008). Biobanking and Ethnic Monitoring. In Darryl R. J. Macer (ed.), Asia-Pacific Perspectives on Biotechnology and Bioethics. Unesco Bangkok. 1952.
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  3. Isabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, Jenny Duchier, Brigitte Jansen, Jürgen Simon, Paula Lobatao De Faria, Anna Perez-Lezaun, Bert Visser, Garrath D. Williams, Anne Cambon-Thomsen & The Eurogenbank Consortium, An Empirical Survey on Biobanking of Human Genetic Material and Data in Six EU Countries.
    Biobanks correspond to different situations: research and technological development, medical diagnosis or therapeutic activities. Their status is not clearly defined. We aimed to investigate human biobanking in Europe, particularly in relation to organisational, economic and ethical issues in various national contexts. Data from a survey in six EU countries were collected as part of a European Research Project examining human and non-human biobanking . A total of 147 institutions concerned with biobanking of human samples and data were investigated by questionnaires (...)
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  4. Jürgen Simon (1999). Rechtliche Aspekte der Präimplantationsdiagnostik in Europa. Ethik in der Medizin 11 (1):62-69.
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