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Early Check: Expanded Screening in Newborns
spinal muscular atrophy, fragile x syndrome, fragile x - premutation, duchenne muscular dystrophy, hyperinsulinemic hypoglycemia, familial 1, diabetes mellitus, adrenoleukodystrophy, neonatal, medium-chain acyl-coa dehydrogenase deficiency, very long chain acyl coa dehydrogenase deficiency, beta-ketothiolase deficiency, severe combined immunodeficiency due to adenosine deaminase deficiency, primary hyperoxaluria type 1
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