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Date: 2014-10-30 12:17:31Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Biotinidase deficiency Isovaleric acidemia Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Congenital hypothyroidism Health Rare diseases Genetic genealogy | NOTICE OF PROPOSED RULEMAKINGAdd to Reading ListSource URL: www.azdhs.govDownload Document from Source WebsiteFile Size: 88,35 KBShare Document on Facebook |