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Direct‐to‐consumer genetic testing: Perspectives on its value in healthcare

30 Oct 2015

Abstract excerpt

The direct-to-consumer genetic testing debate reached a fever pitch in November 2013 when the US Food and Drug Administration (FDA) instructed 23andMe to discontinue marketing and sale of their Personal Genome Service. In 2015, 23andMe emerged with FDA approval to market a carrier test for Bloom syndrome only, and plans to release additional reports. The dust has settled and it is time to ask: What have we...

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PMID: 26517013
DOI: 10.1002/cpt.287

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