Genomic Sequencing Detects Risks in Seemingly Healthy Newborns Genomic Sequencing Detects Risks in Seemingly Healthy Newborns
Newborn genomic sequencing (nGS) can identify risk and carrier status for a wide range of conditions not detectable by currently available newborn screening assays or predicted based on an infant ' s clinical or family history, researchers say.Reuters Health Information
Source: Medscape Pathology Headlines - Category: Pathology Tags: Pediatrics News Source Type: news
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