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Date: 2009-02-03 16:51:23Medical genetics Argininosuccinic aciduria Urea cycle disorder Newborn screening Argininosuccinate lyase Carbamoyl phosphate synthetase I deficiency Glutaric acidemia type 2 Health Rare diseases Genetic genealogy | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)Add to Reading ListSource URL: health.mo.govDownload Document from Source WebsiteFile Size: 18,26 KBShare Document on Facebook |