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PIONEERING STUDIES SHOW PROMISE IN SEQUENCING A BABY’S GENOME AT BIRTH

Early results from North Carolina and New York show that genome sequencing is
catching conditions not found through traditional newborn screening.

By Mark Johnson
June 17, 2024 at 5:00 a.m. EDT

By participating in North Carolina’s Early Check genome study, Matthew Vogt and
Tiffany King learned that their daughter, Fern, seen here, has a gene mutation
linked to a syndrome that can affect her hearing. (Kate Medley/for The
Washington Post)

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RALEIGH, N.C. — Tiffany King had given birth to her daughter, Fern, a little
more than a month earlier and was back at her job as a construction manager when
the phone rang. The caller said she had news about the infant’s genome, the
complex genetic code found in virtually every human cell.


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