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Methylcrotonyl-CoA
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#	Item
21	Microsoft Word - Haitian_Rhode_Island_insert.doc Add to Reading List Source URL: 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
22	Overview of Newborn Screening for Organic Acidemias – For Parents What is newborn screening? Before babies go home from the nursery, they have a small amount of blood taken from their heel to test for a group of condit Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-22 10:08:32 Genetic genealogy Isovaleric acidemia Newborn screening Organic acidemia Glutaric aciduria type 1 Methylmalonic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Metabolism Acidosis Health Rare diseases Medicine
23	Microsoft Word - Rhode Island Insert English FINAL.doc Add to Reading List Source URL: 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
24	Microsoft Word - Haitian_New_Hampshire_Insert.doc Add to Reading List Source URL: 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
25	3-Methylcrotonyl-CoA Carboxylase Deficiency (3-MCC) 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 10:28:48 Epidemiology Newborn screening Screening Methylcrotonyl-CoA carboxylase Health Medicine Pediatrics
26	CHAPTER 66 PDF p. 1 of 3 CHAPTER 66 (SB 24) Add to Reading List Source URL: www.lrc.ky.gov Language: English - Date: 2005-07-07 13:26:35 Newborn screening Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Short-chain acyl-coenzyme A dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Health Medicine Rare diseases
27	Hypermethioninemia (MET) What problems can Hypermethioninemia cause? What is a positive newborn screen? Newborn screening is done on tiny samples of Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 20:45:56 Rare diseases Medical tests Epidemiology Newborn screening Screening Protein Hypermethioninemia Infant 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Pediatrics
28	2012 Minnesota Department of Health 3-MCC Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:16 Rare diseases Coenzymes 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Methylcrotonyl-CoA Carnitine MCC Hypoglycemia Biotinidase deficiency Health Medicine Methylcrotonyl-CoA carboxylase
29	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
30	A Guide for Prenatal Educators This booklet is made possible by & Add to Reading List Source URL: 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