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...
| Main Author: | |
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| Format: | Electronic Article |
| Language: | English |
| Check availability: | HBZ Gateway |
| Journals Online & Print: | Drawer...
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| Fernleihe: | Fernleihe für die Fachinformationsdienste |
| Published: |
Wiley-Blackwell
[2016]
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| In: |
Bioethics
Year: 2016, Volume: 30, Issue: 8, Pages: 628-635 |
| RelBib Classification: | NCH Medical ethics ZB Sociology |
| Further subjects: | B
Ethics
B genetic counselling B cancer susceptibility B genetic test decliners B Moral Identity B right not to know B social implications |
| Online Access: |
Volltext (Verlag) Volltext (doi) |