2-Methylbutyryl-CoA

Results: 23



#Item
21Rare 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

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
22Rare 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

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
23Rare 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

MISSISSIPPI STATE DEPARTMENT OF HEALTH Newborn Screening Report[removed] AUTHORS AND CONTRIBUTORS

Add to Reading List

Source URL: msdh.ms.gov

Language: English - Date: 2011-11-18 10:10:08
UPDATE