<--- Back to Details
| First Page | Document Content | |
|---|---|---|
 Date: 2013-07-08 12:47:26Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine |
Add to Reading List |
Newborn Screening Program Disorders | IMD Program List of Disorders, Covered Drugs, Supplements and Specialty FoodsDocID: 1qvPf - 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 |
| Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)DocID: HYMS - View Document |
| Microsoft Word - Organic_Acidemias.docDocID: HMKf - View Document |