First Page | Document Content | |
---|---|---|
Date: 2012-04-12 12:46:55Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy | Microsoft Word - MoD Fact Sheet 2011Add to Reading ListSource URL: azdhs.govDownload Document from Source WebsiteFile Size: 78,38 KBShare Document on Facebook |
Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received InitialDocID: 14zTU - View Document | |
TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhDDocID: 12v8A - View Document | |
Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findingsDocID: 12jOC - View Document | |
Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received InitialDocID: 11G3r - View Document | |
Microsoft Word - Newborn Screening framework_FINAL.docDocID: U9E1 - View Document |