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Genetic genealogy / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Biotinidase deficiency / Maple syrup urine disease / Glutaric aciduria type 1 / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine
Date: 2011-07-21 16:18:35
Genetic genealogy
Newborn screening
Propionic acidemia
Methylmalonic acidemia
Isovaleric acidemia
Biotinidase deficiency
Maple syrup urine disease
Glutaric aciduria type 1
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Health
Rare diseases
Medicine

Agency of Human Services  Division of Maternal and Child Health  Children with Special Health Needs  Vermont Newborn Screening Program REFUSAL TO CONSENT TO NEWBORN SCREENING

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