First Page | Document Content | |
---|---|---|
Date: 2011-12-12 15:42:57Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Hepatology Epidemiology Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy | Microsoft Word - pocket facts.docxAdd to Reading ListSource URL: ndhealth.govDownload Document from Source WebsiteFile Size: 51,98 KBShare Document on Facebook |
American College of Medical Genetics ACT SHEET Newborn Screening ACT SheetDocID: 1u7Bc - View Document | |
HEARING MATTERS Newborn Hearing Screening 2.0 By Nina Kraus, PhD, & Travis White-Schwoch UDocID: 1tKwJ - View Document | |
American College of Medical Genetics ACT SHEET Newborn Screening ACT SheetDocID: 1sTqf - View Document | |
Department of Health REGIONAL OFFICE IV-A CALABARZON LIST OF NEWBORN SCREENING FACILITIES CodeDocID: 1s9vP - View Document | |
KY DLS Reference List of Tests Contents Acylcarnitines ................................................................................................................................................ 1 Adenovirus .......DocID: 1rdo4 - View Document |