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Genetic 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
Date: 2011-07-21 16:18:35
Genetic 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

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 

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Source URL: healthvermont.gov

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