First Page | Document Content | |
---|---|---|
Date: 2014-09-09 13:55:11Pediatrics Mental retardation Epidemiology Newborn screening Phenylketonuria Galactosemia Isovaleric acidemia 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Rare diseases | Annual Report2012_corrected.pubAdd to Reading ListSource URL: michigan.govDownload Document from Source WebsiteFile Size: 226,49 KBShare Document on Facebook |
NEWSLETTER SPRING-2015-Final.pubDocID: 180UV - View Document | |
Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received InitialDocID: 14zTU - View Document | |
CDC’s Role in the Implementation of Newborn Screening Pilot Programs Activities of the Newborn Screening and Molecular Biology Branch Carla D. Cuthbert, Ph.D.DocID: 12A2f - 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 |