![Medical genetics / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Biotinidase deficiency / Glutaric aciduria type 1 / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy Medical genetics / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Biotinidase deficiency / Glutaric aciduria type 1 / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy](https://www.pdfsearch.io/img/a574a01d767d1fff48bb7937d7bb222a.jpg) Date: 2012-04-12 12:46:54Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy | | OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTEAdd to Reading ListSource URL: azdhs.govDownload Document from Source Website File Size: 46,58 KBShare Document on Facebook
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