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Methylcrotonyl-CoA
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#	Item
51	Microsoft Word - Vermont Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2008-04-01 13:39:57 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
52	Microsoft Word - Haitian_New_Hampshire_Insert.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:10 Medical genetics Propionic acidemia Methylcrotonyl-CoA carboxylase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Methylcrotonyl-CoA Acyl CoA dehydrogenase Malonyl-CoA decarboxylase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
53	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 16:37:49 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
54	Microsoft Word - Rhode Island Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:25 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
55	Microsoft Word - Haitian_Rhode_Island_insert.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:30 Medical genetics Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylcrotonyl-CoA Very long-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase Acyl-CoA dehydrogenase Methylmalonic acidemia Health Rare diseases Genetic genealogy
56	State of Illinois Illinois Department of Public Health Newborn Screening Practitioner’s Manual January 2011 Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2011-05-31 16:09:41 Medical tests Mental retardation Medical genetics Epidemiology Newborn screening Maternal and Child Health Bureau Screening Galactosemia 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Pediatrics
57	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:47:40 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Fatty-acid metabolism disorder 3-Methylcrotonyl-CoA carboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
58	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 16:38:00 Rare diseases Newborn screening Fatty-acid metabolism disorder Biotinidase deficiency Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine palmitoyltransferase I 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Health Genetic genealogy Medical genetics
59	A Guide for Prenatal Educators This booklet is made possible by & Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2014-03-24 17:53:47 Pediatrics Rare diseases Inborn errors of carbohydrate metabolism B vitamins Epidemiology Newborn screening Phenylketonuria 3-Methylcrotonyl-CoA carboxylase deficiency Galactosemia Health Medicine Genetic genealogy
60	Disease Name 3-methylcrotonyl-CoA carboxylase deficiency Alternate name(s) Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 11:48:25 3-Methylcrotonyl-CoA carboxylase deficiency Rare diseases Coenzymes Newborn screening Methylcrotonyl-CoA carboxylase Hepatology Methylcrotonyl-CoA Carnitine Asymptomatic Health Medicine Pediatrics