Genetic Moralism and Health
This article examines the moralistic language and arguments used in relation to genetics. The focus is on three practices: (1) the claims that there is a duty to know about one’s own genetic makeup, (2) assertions that genetic information should be used to inform reproductive decisions, and (3) the...
Κύριος συγγραφέας: | |
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Τύπος μέσου: | Ηλεκτρονική πηγή Άρθρο |
Γλώσσα: | Αγγλικά |
Έλεγχος διαθεσιμότητας: | HBZ Gateway |
Journals Online & Print: | |
Fernleihe: | Fernleihe für die Fachinformationsdienste |
Έκδοση: |
Cambridge Univ. Press
2019
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Στο/Στη: |
Cambridge quarterly of healthcare ethics
Έτος: 2019, Τόμος: 28, Τεύχος: 2, Σελίδες: 225-235 |
Άλλες λέξεις-κλειδιά: | B
Informed Consent
B Reproduction B Biobanks B Genetic Information B Moralism B Genetics |
Διαθέσιμο Online: |
Volltext (lizenzpflichtig) Volltext (lizenzpflichtig) |
Σύνοψη: | This article examines the moralistic language and arguments used in relation to genetics. The focus is on three practices: (1) the claims that there is a duty to know about one’s own genetic makeup, (2) assertions that genetic information should be used to inform reproductive decisions, and (3) the proposition that there are moral reasons to participate in biobank research. With these three, the author contends that there are equally good, if not better, arguments to challenge them from a Millian perspective. Furthermore, especially in the current political climate, there is a need to respect people’s privacy concerns. |
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ISSN: | 1469-2147 |
Περιλαμβάνει: | Enthalten in: Cambridge quarterly of healthcare ethics
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Persistent identifiers: | DOI: 10.1017/S0963180119000070 |