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Date: 2012-03-28 12:35:21Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Propionic acidemia Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy | Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia IsobutyrylglycinuriaAdd to Reading ListSource URL: msdh.ms.govDownload Document from Source WebsiteFile Size: 466,84 KBShare Document on Facebook |
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