<--- Back to Details
First PageDocument Content
Rare diseases / Isovaleric acidemia / Glutaric acidemia type 2 / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Methylmalonic acidemia / Glutaric aciduria type 1 / Acyl CoA dehydrogenase / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Propionic acidemia / Health / Genetic genealogy / Medical genetics
Date: 2007-10-17 09:00:32
Rare diseases
Isovaleric acidemia
Glutaric acidemia type 2
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Methylmalonic acidemia
Glutaric aciduria type 1
Acyl CoA dehydrogenase
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Propionic acidemia
Health
Genetic genealogy
Medical genetics

Microsoft Word - Haitian_Maine_Insert.doc

Add to Reading List

Source URL: nergg.org

Download Document from Source Website

File Size: 11,74 KB

Share Document on Facebook

Similar Documents

Newborn screening / Isovaleric acidemia / Galactosemia / Methylmalonic acidemia / Propionic acidemia / Malonyl-CoA decarboxylase deficiency / Inborn error of metabolism / Argininosuccinic aciduria / Organic acidemia / Health / Rare diseases / Medicine

TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD

DocID: 12v8A - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Propionic acidemia / Methylmalonic acidemia / Fatty-acid metabolism disorder / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Galactosemia / Malonyl-CoA decarboxylase deficiency / Health / Rare diseases / Genetic genealogy

Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings

DocID: 12jOC - View Document

Propionic acidemia / Propionyl-CoA carboxylase / Genetic testing / Prenatal diagnosis / Health / Medicine / Rare diseases

J Med Genet 1999;36:412–[removed]Short reports

DocID: NHX0 - View Document

Medical genetics / Methylmalonic acidemia / Glutaric aciduria type 1 / Hyperlysinemia / Propionic acidemia / Health care provider / Insurance / Health / Rare diseases / Genetic genealogy

2013 General Session - Introduced Version - HB0145 - Insurance-coverage of phenylketonuria.

DocID: NC55 - View Document

Medical genetics / Methylmalonic acidemia / Glutaric aciduria type 1 / Hyperlysinemia / Health care provider / Propionic acidemia / Health / Rare diseases / Genetic genealogy

2013 General Session - Engrossed Version - HB0145 - Insurance-coverage of inherited enzymatic disorders.

DocID: NxPs - View Document