<--- Back to Details
First PageDocument Content
Medical genetics / Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Propionic acidemia / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Acyl CoA dehydrogenase / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Genetic genealogy
Date: 2014-12-15 13:01:02
Medical genetics
Newborn screening
Isovaleric acidemia
Methylmalonic acidemia
Propionic acidemia
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Fatty-acid metabolism disorder
Acyl CoA dehydrogenase
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Health
Rare diseases
Genetic genealogy

Disorders and Reference Ranges

Add to Reading List

Source URL: azdhs.gov

Download Document from Source Website

File Size: 103,94 KB

Share Document on Facebook

Similar Documents

DOCX Document

DocID: 1wwhs - View Document

DOCX Document

DocID: 1wv76 - View Document

PDF Document

DocID: 1w4hN - View Document

-Application for Renewal of RDMM Catalyst Grants This application is to be used by the Network’s Scientific Advisory Committee (SAC) to determine as to whether to provide an additional year of funding ($

DocID: 1vceh - View Document

MULTISYSTEMIC RARE DISEASES

DocID: 1v3AN - View Document