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Genetic genealogy / Fatty-acid metabolism disorder / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Propionic acidemia / Malonyl-CoA decarboxylase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine
Date: 2013-07-08 12:47:26
Genetic genealogy
Fatty-acid metabolism disorder
Newborn screening
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Carnitine-acylcarnitine translocase deficiency
Propionic acidemia
Malonyl-CoA decarboxylase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Health
Rare diseases
Medicine

Newborn Screening Program Disorders

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