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Date: 2008-04-01 13:39:57Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy | Microsoft Word - Vermont Insert English FINAL.docAdd to Reading ListSource URL: nergg.orgDownload Document from Source WebsiteFile Size: 17,20 KBShare Document on Facebook |
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