Newborn screening panels aim to identify genetic disorders early in life , allowing for timely intervention and improved health outcomes. The use of genomics in newborn screening can facilitate the detection of a broad range of conditions, enabling more accurate and comprehensive testing. Genet offers services to support the development and implementation of recommended newborn screening panels, helping to advance the field of genetic testing and improve the quality of care for newborns and their families.
Recommended Newborn Screening Panels
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