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Methylcrotonyl-CoA carboxylase
Results: 68

#	Item
41	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: 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
42	Vermont routinely screens newborns for 29 conditions. They are: • • • • Add to Reading List Source URL: healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Glutaric aciduria type 1 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
43	Vermont routinely screens newborns for 29 conditions. They are: • • • • Add to Reading List Source URL: www.healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Glutaric aciduria type 1 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
44	Arizona Administrative Register / Secretary of State Notices of Final Rulemaking NOTICES OF FINAL RULEMAKING The Administrative Procedure Act requires the publication of the final rules of the state’s agencies. Final r Add to Reading List Source URL: azdhs.gov Language: English - Date: 2014-05-29 18:43:12 Pediatrics Newborn screening Biotinidase deficiency Methylmalonic acidemia Congenital hypothyroidism Propionic acidemia Galactosemia Health care provider 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Rare diseases
45	Arizona Administrative Register / Secretary of State Notices of Final Rulemaking NOTICES OF FINAL RULEMAKING The Administrative Procedure Act requires the publication of the final rules of the state’s agencies. Final r Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2014-05-29 18:43:12 Pediatrics Newborn screening Biotinidase deficiency Methylmalonic acidemia Congenital hypothyroidism Propionic acidemia Galactosemia Health care provider 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Rare diseases
46	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
47	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:06 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylcrotonyl-CoA carboxylase Propionic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
48	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
49	Microsoft Word - Rhode Island insert Khmer.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:33 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Mitochondrial trifunctional protein deficiency Methylcrotonyl-CoA 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
50	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

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