상세정보
- 상세정보
The Right to Know and the Right Not to Know :Genetic Privacy and Responsibility
Chadwick, Ruth
- 책이미지
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- 도서 상세정보
| 자료유형 | e-Book |
|---|---|
| 개인저자 | Chadwick, Ruth, editor of compilation. Levitt, Mairi, editor of compilation. Shickle, Darren, editor of compilation. |
| 서명/저자사항 | The Right to Know and the Right Not to Know :Genetic Privacy and Responsibility :Edited by Ruth Chadwick, Mairi Levitt, Darren Shickle. |
| 판사항 | 2nd ed. |
| 발행사항 | Cambridge:Cambridge University Press,2014. |
| 형태사항 | 1 online resource (232 pages) :digital, PDF file(s). |
| 총서사항 | Cambridge Bioethics and Law. |
| 총서부출표목 | Cambridge Bioethics and Law. |
| 기타형태 저록 | Print version, 9781107076075 |
| ISBN | 9781139875981 (ebook) |
| 일반주기 | Title from publisher's bibliographic system (viewed on 12 Aug 2015). |
| 요약 | The privacy concerns discussed in the 1990s in relation to the New Genetics failed to anticipate the relevant issues for individuals, families, geneticists and society. Consumers, for example, can now buy their personal genetic information and share it online. The challenges facing genetic privacy have evolved as new biotechnologies have developed, and personal privacy is increasingly challenged by the irrepressible flow of electronic data between the personal and public spheres and by surveillance for terrorism and security risks. This book considers the right to know and the right not to know about your own and others' genomes. It discusses new privacy concerns and developments in ethical thinking, with the greater emphasis on solidarity and equity. The multidisciplinary approach covers current topics such as biobanks and forensic databases, DIY testing, group rights and accountability, the food we eat and the role of the press and the new digital media. |
| 일반주제명 | Genetic disorders--Diagnosis--Moral and ethical aspects Genetic screening--Law and legislation Human chromosome abnormalities--Diagnosis--Moral and ethical aspects LAW / Health.--bisacsh Privacy, Right of |
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