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Medical genetics / Fatty-acid metabolism disorder / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hyperammonemia / Carnitine / Isovaleric acidemia / Health / Rare diseases / Genetic genealogy
Date: 2011-02-25 12:37:37
Medical genetics
Fatty-acid metabolism disorder
Newborn screening
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Carnitine-acylcarnitine translocase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Hyperammonemia
Carnitine
Isovaleric acidemia
Health
Rare diseases
Genetic genealogy

STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM

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Source URL: health.state.tn.us

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