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Date: 2009-02-03 16:52:02Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Methylcrotonyl-CoA carboxylase Biotinidase deficiency Propionic acidemia Health Genetic genealogy Medical genetics | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)Add to Reading ListSource URL: health.mo.govDownload Document from Source WebsiteFile Size: 18,95 KBShare Document on Facebook |