The ethics of genetic screening
著者
書誌事項
The ethics of genetic screening
Kluwer Academic Publishers, c1999
大学図書館所蔵 全3件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references and index
内容説明・目次
内容説明
This collection of essays represents the work produced in the course of a three-year project funded by the Commission of the European Communities under the Biomed I programme, on the ethics of genetic screening, entitled 'Genetic screening: ethical and philosophical perspectives, with special reference to multifactorial diseases'. The short title of the project was Euroscreen, thereafter known as Euroscreen I, in the light of the fact that a second project on genetic screening was subsequently funded. The project was multinational and multidisciplinary, and had as its objectives to examine the nature and extent of genetic screening programmes in different European countries; to analyse the social policy response to these developments in different countries; and to explore the applicability of normative ethical frameworks to the issues. The project was led by a core group who had oversight of the project and members of which have acted as editors for this volume. Darren Shickle edited the first section; Henk ten Have the second; Ruth Chadwick and Urban Wiesing the third and final part. The volume opens with an overview of genetic screening and the principles available for addressing developments in the field, with special reference to the Wilson and Jungner principles on screening. The first of the three major sections thereafter includes papers on the state of the art in different countries, together with some analysis of social context and policy.
目次
- Contributors. Preface. The Wilson and Jungner Principles of Screening and Genetic Testing
- D. Shickle. Genetic screening, information and counselling in Austria
- G. Hauser.The Belgian perspective on genetic screening
- K. Dierickx. Thalassemia prevention in Cyprus. Past, present and future
- P. Ioannou. Some developments in genetic screening in Finland
- V. Launis. Genetic screening: Ethical debates and regulatory systems in France
- A. Boue. Screening in Germany: Carrier screening, pre-natal care and other screening projects
- T. Schroeder-Kurth. Population screening in Greece for prevention of genetic diseases
- C. Metaxotou, A. Mavrou. Ethics and genetic screening in the Republic of Ireland
- D. Dooley. Genetic screening in the Netherlands. The state of the debate
- R. Hoedemaekers. Genetic screening and genetic services in Slovakia
- V. Ferak. Historical and social background. Introduction
- H. ten Have. From eugenics to genetic screening. Historical problems of human genetic applications
- H.-P. Kroener. Genetics in Germany. History and hysteria
- U. Wiesing. A sociological perspective on genetic screening
- M. Levitt. Moral and philosophical issues. Introduction
- R.F. Chadwick, U. Wiesing. Genetic information and care
- I. Poern. Genetic screening, genetic testing and privacy
- J. Sandor. Reconciling liberty and the common good? Genetic screening in the Republic of Ireland
- D. Dooley. Genetic screening and testing. A moral map
- R. Hoedemaekers. The genetic testing of children
- A. Clarke. Index.
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