Overview

Genetic Databases current regulatory frameworks for and policy debates about genetic databases and challenges the prevailing orthodoxy of
Read More Show Less
... See more details below
Genetic Databases

Available on NOOK devices and apps  
  • NOOK Devices
  • Samsung Galaxy Tab 4 NOOK
  • NOOK HD/HD+ Tablet
  • NOOK
  • NOOK Color
  • NOOK Tablet
  • Tablet/Phone
  • NOOK for Windows 8 Tablet
  • NOOK for iOS
  • NOOK for Android
  • NOOK Kids for iPad
  • PC/Mac
  • NOOK for Windows 8
  • NOOK for PC
  • NOOK for Mac
  • NOOK for Web

Want a NOOK? Explore Now

NOOK Book (eBook)
$59.95
BN.com price

Overview

Genetic Databases current regulatory frameworks for and policy debates about genetic databases and challenges the prevailing orthodoxy of
Read More Show Less

Product Details

  • ISBN-13: 9780203577929
  • Publisher: Routledge
  • Publication date: 3/18/2004
  • Sold by: Barnes & Noble
  • Format: eBook
  • File size: 724 KB

Meet the Author

Oonagh Corrigan is a sociologist with a research interest in social and ethical issues surrounding developments in genetics and the pharmaceutical industry. In particular much of her work to date has focussed on the implications for human subjects involved in biomedical research and on regulatory mechanisms designed to protect such subjects.

Richard Tutton is a research fellow in the Science and Technology Studies Unit (SATSU) in the Department of Sociology at the University of York. He has been researching the various social and ethical implications of developments in human genetics for several years
Read More Show Less

Table of Contents

1. Introduction: Public Participation in Genetic Databases 2. Persons, Property and Gift: Exploring Languages of Tissue Donation to Biomedical Research 3. Blood Donation for Genetic Research: What Can we Learn From Donor's Narratives? 4. Levels and Styles of Participation in Genetic Databases: A Case Study of the North Cumbria Community Genetics Project 5. Informed Consent: The Contradictory Ethical Safeguards in Pharmacogenetics 6. Ambiguous Gifts: Public Anxiety, Informed Consent and Biobanks 7. Abandoning Informed Consent - The Case of Genetic Research in Population Collections 8. Children's Participation in Genetic Epidemiology: Consent and Control 9. 'Public Consent' or 'Scientific Citizenship'? What Counts as Public Participation in Population Based DNA Collections? 10. Tissue Collection and the Pharmaceutical Industry: Investigating Corporate Biobanks
Read More Show Less

Customer Reviews

Be the first to write a review
( 0 )
Rating Distribution

5 Star

(0)

4 Star

(0)

3 Star

(0)

2 Star

(0)

1 Star

(0)

    If you find inappropriate content, please report it to Barnes & Noble
    Why is this product inappropriate?
    Comments (optional)