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Date: 2011-12-12 15:42:57Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Hepatology Epidemiology Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy | Microsoft Word - pocket facts.docxAdd to Reading ListSource URL: ndhealth.govDownload Document from Source WebsiteFile Size: 51,98 KBShare Document on Facebook |
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Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)DocID: HYMS - View Document | |
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)DocID: HA0p - View Document | |
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Fetal Fatty Acid Oxidation Defects and Maternal Liver Disease in Pregnancy Marsha F. Browning, MD, MPH, Harvey L. Levy, Cecilia Larson, MD, and Vivian E. Shih, MD OBJECTIVE: The objective was to evaluate the relationshipDocID: ErYn - View Document |