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 Date: 2011-07-21 16:18:35Genetic genealogy Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Maple syrup urine disease Glutaric aciduria type 1 Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine |
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Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT to REPEAT NEWBORN SCREENING