Assessing Genetic Risks:

Implications for Health and Social Policy

Status: Available Now

Size: 352 pages, 6 x 9

Publication Year:1994

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PAPERBACK ISBN-10: 0-309-08660-4 ISBN-13: 978-0-309-08660-8	$90.00	Add to Cart

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Authors:
Lori B. Andrews, Jane E. Fullarton, Neil A. Holtzman, and Arno G. Motulsky, Editors; Committee on Assessing Genetic Risks, Institute of Medicine
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Description:
Raising hopes for disease treatment and prevention, but also the specter of discrimination and "designer genes," genetic testing is potentially one of the most socially explosive developments of our time. This book presents a current assessment of this rapidly evolving ...
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"...it reads quickly and easily and the underlying messages are undoubtedly of international relevance."--Canadian Medical Association Journal
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Table of Contents
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Front Matter	i-xiv
Exective Summary	1-28	(skim)
1 Setting the Stage	29-58	(skim)
2 Genetic Testing and Assessment	59-115	(skim)
3 Laboratory Issues in Human Genetics	116-145	(skim)
4 Issues in Genetic Counseling	146-184	(skim)
5 Public Education in Genetics	185-201	(skim)
6 Personnel Issues in Human Genetics	202-233	(skim)
7 Financing of Genetic Testing and Screening Services	234-246	(skim)
8 Social, Legal, and Ethical Implications of Genetic Testing	247-289	(skim)
9 Research and Policy Agenda	290-308	(skim)
Appendix A: Workshop Participants	309-316	(skim)
Appendix B: Committee Biographies	317-324	(skim)
Index	325-338	(skim)

Description

Raising hopes for disease treatment and prevention, but also the specter of discrimination and "designer genes," genetic testing is potentially one of the most socially explosive developments of our time. This book presents a current assessment of this rapidly evolving field, offering principles for actions and research and recommendations on key issues in genetic testing and screening.

Advantages of early genetic knowledge are balanced with issues associated with such knowledge: availability of treatment, privacy and discrimination, personal decisionmaking, public health objectives, cost, and more. Among the important issues covered:

Quality control in genetic testing.
Appropriate roles for public agencies, private health practitioners, and laboratories.
Value-neutral education and counseling for persons considering testing.
Use of test results in insurance, employment, and other settings.