First Page | Document Content | |
---|---|---|
Date: 2011-10-11 08:14:49Genetic genealogy Newborn screening Methylmalonic acidemia Propionic acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Health Rare diseases Medicine | Newborn Screening BrochureAdd to Reading ListSource URL: www.wadsworth.orgDownload Document from Source WebsiteFile Size: 317,51 KBShare Document on Facebook |
IMD Program List of Disorders, Covered Drugs, Supplements and Specialty FoodsDocID: 1qvPf - View Document | |
KIRI SUNDE Class of 2012 Holland, MI “DocID: 15n5H - View Document | |
Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition IncidenceDocID: Z5KR - View Document | |
2013 General Session - Introduced Version - HB0145 - Insurance-coverage of phenylketonuria.DocID: NC55 - View Document | |
2013 General Session - Engrossed Version - HB0145 - Insurance-coverage of inherited enzymatic disorders.DocID: NxPs - View Document |