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Genotyping in clinical trials: Towards a principle of informed request
Journal of Medicine and Philosophy 23 (3):288 – 296 (1998)
Abstract
This paper reviews the usefulness of bioethical instruments such as the informed consent principle to handle ethical and political challenges of clinical trials in genotyping and DNA-banking and discusses an informed request model as well as other contractual relations between research institutions, patients, and their families.Author's Profile
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Citations of this work
An empirical survey on biobanking of human genetic material and data in six EU countries.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 - 2003 - European Journal of Human Genetics 11:475–488.
Ethical aspects of genome diversity research: genome research into cultural diversity or cultural diversity in genome research? [REVIEW]Ilhan Ilkilic & Norbert W. Paul - 2009 - Medicine, Health Care and Philosophy 12 (1):25-34.
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