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Medical genetics / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Biotinidase deficiency / Glutaric aciduria type 1 / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy
Date: 2012-04-12 12:46:54
Medical genetics
Newborn screening
Propionic acidemia
Methylmalonic acidemia
Isovaleric acidemia
Biotinidase deficiency
Glutaric aciduria type 1
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Health
Rare diseases
Genetic genealogy

OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE

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