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Human genome research and the public interest: progress notes from an American science policy experiment.

机译:人类基因组研究与公共利益:美国科学政策实验的进展记录。

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摘要

This essay reviews the efforts of the U.S. Human Genome Project to anticipate and address the ethical, legal, and social implications of new advances in human genetics. Since 1990, approximately $10 million has been awarded by the National Institutes of Health and the Department of Energy, in support of 65 research, education, and public discussion projects. These projects address four major areas of need: (1) the need for both client-centered assessments of new genetic services and for improved knowledge of the psychosocial and ethnocultural factors that shape clients' clinical genetic experiences; (2) the need for clear professional policies regarding human-subject research, clinical practice standards, and public health goals in human genetics; (3) the need for social policy protection against unfair access to and use of personal genetic information; and (4) the need for improved public and professional understanding and discussion of these issues. The Human Genome Project's goal is to have defined, by 1995, policy options and programs capable of addressing these needs.
机译:本文回顾了美国人类基因组计划在预测和解决人类遗传学新进展的伦理,法律和社会影响方面的工作。自1990年以来,美国国立卫生研究院和能源部共拨款约1000万美元,以支持65个研究,教育和公共讨论项目。这些项目解决了四个主要需求领域:(1)需要以客户为中心的新遗传服务评估,以及对影响客户临床遗传经验的社会心理和民族文化因素的了解; (2)需要制定有关人类受试者研究,临床实践标准和人类遗传学公共卫生目标的明确专业政策; (3)需要采取社会政策保护措施,以防止不公正地获取和使用个人遗传信息; (4)需要提高公众和专业人士对这些问题的理解和讨论。人类基因组计划的目标是在1995年之前确定能够满足这些需求的政策选择和计划。

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