Paperback / softback | |
January 21, 2004 | |
9780801879265 | |
English | |
312 | |
9.00 Inches (US) | |
6.00 Inches (US) | |
0.81 Inches (US) | |
1.04 Pounds (US) | |
$35.00 USD, £26.00 GBP | |
v2.1 Reference | |
The Double-Edged Helix
Social Implications of Genetics in a Diverse Society
The Double-Edged Helix explores the impact of recent genetic discoveries on both different population segments and society as a whole. The authors address the medical and ethical implications of the new technologies, outlining potential positive and negative effects of genetic research on minorities, individuals with disabilities, and those of diverse sexual orientations. Presenting a wide array of perspectives, this book emphasizes the need to ensure that research into genetics research does not result in discrimination against people on the basis of their DNA.
About the Authors
Joseph S. Alper, Ph.D., is a professor in the Department of Chemistry at the University of Massachusetts. Catherine Ard, M.M.H.S., is a doctoral candidate in the Heller School for Social Policy and Management at Brandeis University. Adrienne Asch, Ph.D., is the Henry Luce Professor in Biology, Ethics, and the Politics of Human Reproduction at Wellesley College. Jon Beckwith, Ph.D., is American Cancer Society Research Professor of Microbiology and Molecular Genetics at Harvard Medical School. Peter Conrad, Ph.D., is the Harry Coplan Professor of Social Sciences at Brandeis University. Lisa N. Geller, Ph.D., J.D., is an associate at Fish and Richardson, P.C., in Boston.
Reviews
Bringing the concerns of different communities together in a single volume makes it possible to appreciate the mosaic of human issues more fully and forces us to anticipate the challenges that may arise—and that will require our attention—as the genetic revolution proceeds... A much needed antidote to the current genetic hoopla.
A cautious look at the effects of genetic discoveries on society... The issues raised by this book are valid, and all scientists should be aware of them. I often found myself nodding in agreement.
The authors present several thought-provoking issues in regard to prenatal genetic screening and selective abortion. It's a great contribution to the field.
This book superbly and successfully fills its purpose—to show the need for dialogue between researchers, health care professionals, communities, and individuals regarding various aspects of genetic technology.
Johns Hopkins University Press | |
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Paperback / softback | |
January 21, 2004 | |
9780801879265 | |
English | |
312 | |
9.00 Inches (US) | |
6.00 Inches (US) | |
0.81 Inches (US) | |
1.04 Pounds (US) | |
$35.00 USD, £26.00 GBP | |
v2.1 Reference | |
Other Titles by Adrienne Asch
Prenatal Testing and Disability Rights
Other Titles in MEDICAL / Ethics
Handbook for Health Care Ethics Committees, third edition
Bodies in Doubt, second edition
Biomedicine and Beatitude, second edition
Other Titles in Medical ethics & professional conduct
Handbook for Health Care Ethics Committees, third edition
Bodies in Doubt, second edition
The Morehouse Model