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Review
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases

Authors

  1. Correspondence to Dr David Bick, HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA; dbick{at}hudsonalpha.org
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Citation

Bick D, Jones M, Taylor SL, et al
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases

Publication history

  • Received February 25, 2019
  • Accepted March 19, 2019
  • First published April 25, 2019.

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