Providing solutions-defining problems: the imperative of disease prevention in genetic counselling
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- Williams, Clare & Alderson, Priscilla & Farsides, Bobbie, 2002. "Is nondirectiveness possible within the context of antenatal screening and testing?," Social Science & Medicine, Elsevier, vol. 54(3), pages 339-347, February.
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- Barberić Lara, 2013. "Genetic Knowledge and Genetic Reproduction Technologies as New Modes of Governance – are We Witnessing a New Form of Eugenics?," Croatian International Relations Review, Sciendo, vol. 19(69), pages 33-54, December.
- Miller, Fiona Alice & Giacomini, Mita & Ahern, Catherine, 2008. "Contending visions in the evolution of genetic medicine: The case of cancer genetic services in Ontario, Canada," Social Science & Medicine, Elsevier, vol. 67(1), pages 152-160, July.
- Huniche, Lotte, 2011. "Moral landscapes and everyday life in families with Huntington's disease: Aligning ethnographic description and bioethics," Social Science & Medicine, Elsevier, vol. 72(11), pages 1810-1816, June.
- Clarke, Angus & Sarangi, Srikant & Verrier-Jones, Kate, 2011. "Voicing the lifeworld: Parental accounts of responsibility in genetic consultations for polycystic kidney disease," Social Science & Medicine, Elsevier, vol. 72(11), pages 1743-1751, June.
- Weiner, Kate, 2011. "Exploring genetic responsibility for the self, family and kin in the case of hereditary raised cholesterol," Social Science & Medicine, Elsevier, vol. 72(11), pages 1760-1767, June.
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Keywords
Genetic counselling Governmentality Disease prevention Informed consent Non-directiveness Denmark;Statistics
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