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- 資料種別
- 図書
- ISBN
- 9781108473910 hardcover1108473911 hardcover
- 著者・編者
- edited by Britta van Beers, Sigrid Sterckx, Donna Dickenson.
- シリーズタイトル
- 出版事項
- 出版年月日等
- 2018.著作権日付 : ©2018
- 出版年(W3CDTF)
- 2018
- 数量
- xii, 305 pages
- 大きさ
- 24 cm.
- 出版地(国名コード)
- GB
- 本文の言語コード
- eng
- 表現種別
- text
- 機器種別
- unmediated
- キャリア種別
- volume
- 件名標目
- LCC
- DDC
- NDLC
- 対象利用者
- 一般
- 資料の内容に関する注記
- Hippocrates famously advised doctors 'it is far more important to know what person the disease has than what disease the person has'. Yet 2,500 years later, 'personalised medicine', based on individual genetic profiling and the achievements of genomic research, claims to be revolutionary. In this book, experts from a wide range of disciplines critically examine this claim. They expand the discussion of personalised medicine beyond its usual scope to include many other highly topical issues, including: human nuclear genome transfer ('three-parent IVF'), stem cell-derived gametes, private umbilical cord blood banking, international trade in human organs, biobanks such as the US Precision Medicine Initiative, direct-to-consumer genetic testing, health and fitness self-monitoring. Although these technologies often prioritise individual choice, the original ideal of genomic research saw the human genome as 'the common heritage of humanity'. The authors question whether personalised medicine actually threatens this conception of the common good.
- 書誌注記
- Includes bibliographical references and index.
- 所蔵機関
- 国立国会図書館
- 請求記号
- SD81-B65
- 連携機関・データベース
- 国立国会図書館 : 国立国会図書館蔵書
- 書誌ID(NDLBibID)
- 029313423
- LC control number
- 2018022368
- OCLC番号
- 1035771935
- 目録規則
- RDA
- 整理区分コード
- 211