Date: 2011-02-25 12:37:37Medical 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 PROGRAMAdd to Reading ListSource URL: health.state.tn.usDownload Document from Source Website File Size: 51,06 KBShare Document on Facebook
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