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Health Affairs, 27, no. 6 (2008): 1599
doi: 10.1377/hlthaff.27.6.1599
© 2008 by Project HOPE
 
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Genomics

PROLOGUE

Genomics


The first 100 words of the full text of this article appear below.

The mapping of the human genome has created the opportunity for early identification of those at risk for a wide range of common, life-threatening diseases. The pace of discovery in the field of genomic research has been accompanied by expectations that cutting-edge, individualized treatments—so-called personalized medicine—may be just around the corner.

A fundamental question for stakeholders—researchers, policymakers, and consumers alike—is whether these genomic discoveries are useful and can be translated into actual health care interventions that can practically and cost-effectively find their way into hospitals and doctors’ offices.

But how much evidence should be required to show that a discovery . . . [Full Text of this Article]


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