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Ethical Legal and Social Issues of the Human Genome Project: What to Do with What We Know.

机译:人类基因组计划的道德法律和社会问题:如何处理我们所知道的。

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摘要

Since fisal year 1991, the U.S. Human Genome Project has spent $170.6 million in federal funds to help isolate genes associated with Huntington's disease, amyotrophic lateral sclerosis, neurofibromatosis types 1 and 2, myotonic dystrophy, and fragile X syndrome and to localize genes that predispose people to breast cancer, colon cancer, hypertension, diabetes, and Alzheimer's disease. Now comes the hard part. Biology's 21st century megaproject starts to look relatively manageable compared to another challenge facing the enterprise: sorting out ethical, legal, and social issues associated with using this information. "The Human Genome Project," wrote Senior Editor Barbara Jasny in the October 1 Science editorial, stretches "the limits of the technology and the limits of our ability to ethically and rationally apply genetic information to our lives."
机译:自1991财政年度以来,美国人类基因组计划已在联邦基金上花费了1.706亿美元,以帮助分离与亨廷顿氏病,肌萎缩性侧索硬化症,1型和2型神经纤维瘤,肌强直性营养不良和易碎X综合征相关的基因,并定位易感人群的基因乳腺癌,结肠癌,高血压,糖尿病和阿尔茨海默氏病。现在是困难的部分。与企业面临的另一个挑战相比,生物学的21世纪大型项目开始看起来相对可管理:理清与使用此信息相关的道德,法律和社会问题。高级编辑芭芭拉·贾斯尼(Barbara Jasny)在10月1日的《科学》社论中写道:“人类基因组计划”扩展了“技术的局限性以及我们在道德上和理性地将遗传信息应用于我们生活的能力的局限性”。

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