What can we Learn from Patients’ Ethical Thinking about the right ‘not to know’ in Genomics? Lessons from Cancer Genetic Testing for Genetic Counselling
This article is based on a qualitative empirical project about a distinct kinship group who were among the first identified internationally as having a genetic susceptibility to cancer (Lynch Syndrome). 50 were invited to participate (42 were tested; eight declined genetic testing). 15, who had all...
| 1. VerfasserIn: | |
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| Medienart: | Elektronisch Aufsatz |
| Sprache: | Englisch |
| Verfügbarkeit prüfen: | HBZ Gateway |
| Journals Online & Print: | Lade...
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| Fernleihe: | Fernleihe für die Fachinformationsdienste |
| Veröffentlicht: |
Wiley-Blackwell
[2016]
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| In: |
Bioethics
Jahr: 2016, Band: 30, Heft: 8, Seiten: 628-635 |
| RelBib Classification: | NCH Medizinische Ethik ZB Soziologie |
| weitere Schlagwörter: | B
Ethics
B genetic counselling B cancer susceptibility B genetic test decliners B Moral Identity B right not to know B social implications |
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