Even before the sequencing of the human genome began in earnest,Americans started worrying about how information about theirgenetic makeup might be used in harmful ways, and policymakersbegan considering legislation to prevent misuses of geneticinformation. The Genetic Information Nondiscrimination Act,which would prohibit health insurers and employers from askingor requiring a person to take a genetic test and from usinggenetic information in setting insurance rates or making employmentdecisions, passed unanimously in the Senate in 2003 and againin 2005. The bill remained stalled in the House of Representatives,however, apparently because the House leadership . . . [Full Text of this Article]
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Dr. Hudson is the director of the Johns Hopkins Genetics and Public Policy Center, Washington, DC, and an associate professor at the Berman Bioethics Institute, Institute of Genetic Medicine, and Department of Pediatrics at Johns Hopkins University, Baltimore.
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