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2-Methylbutyryl-CoA
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#	Item
11	2-Methylbutyryl-CoA Dehydrogenase Deficiency (2-MBG) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:13:50 Epidemiology Newborn screening Screening 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
12	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2009-02-03 16:52:18 Medical genetics Newborn screening Organic acidemia 2-Methylbutyryl-CoA dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
13	Annual Report2012_corrected.pub Add to Reading List Source URL: michigan.gov Language: English - Date: 2014-09-09 13:55:11 Pediatrics Mental retardation Epidemiology Newborn screening Phenylketonuria Galactosemia Isovaleric acidemia 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Rare diseases
14	Newborn Screening Brochure Add to Reading List Source URL: www.wadsworth.org Language: English - Date: 2011-10-11 08:14:49 Genetic 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
15	Chapter 4 : Newborn Screening Almost every child born in the United States undergoes state-mandated newborn screening. For each state, a small blood sample (“heel stick”) is collected from each newborn within 48 hou Add to Reading List Source URL: www.geneticalliance.org Language: English - Date: 2013-10-04 10:41:36 Genetic genealogy Pediatrics Newborn screening Methylmalonic acidemia Neonatal heel prick Galactosemia Biotinidase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Hyperammonemia Health Medicine Rare diseases
16	Microsoft Word - mso20.doc Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-14 08:02:14 Rare diseases Hypermethioninemia Newborn screening Medical genetics 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medicine Health Genetic genealogy
17	State of Illinois Rod R. Blagojevich, Governor Department of Public Health Eric E. Whitaker, M.D., M.P.H., Director Newborn Metabolic Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2007-07-24 10:41:11 Medical genetics Newborn screening Propionic acidemia Fatty-acid metabolism disorder 2-Methylbutyryl-CoA dehydrogenase deficiency Biotinidase deficiency Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
18	MISSISSIPPI STATE DEPARTMENT OF HEALTH Newborn Screening Report[removed] AUTHORS AND CONTRIBUTORS Add to Reading List Source URL: www.msdh.state.ms.us Language: English - Date: 2011-11-18 10:10:08 Rare diseases Inborn errors of carbohydrate metabolism Epidemiology Newborn screening Galactosemia Screening Phenylketonuria Galactose-1-phosphate uridylyltransferase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
19	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:50 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
20	Microsoft Word - mso20.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 08:02:14 Rare diseases Hypermethioninemia Newborn screening Medical genetics 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medicine Health Genetic genealogy