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How Genome Sequencing Can Broaden the Scope of Newborn Screening

Standard newborn screening can detect dozens of inherited diseases, but genomics technology enables testing for hundreds of them. A North Carolina program evaluating the feasibility of bringing genomics to newborn screening is expanding with an initial goal of testing 5,000 babies in the next year.
University Of North Carolina North Carolina United States Cobey Culton John Merck Fund Harryb Helmsley Charitable

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