<--- Back to Details
First PageDocument Content
Medical genetics / Newborn screening / Organic acidemia / 2-Methylbutyryl-CoA dehydrogenase deficiency / Methylmalonic acidemia / Health / Rare diseases / Genetic genealogy
Date: 2009-02-03 16:52:18
Medical genetics
Newborn screening
Organic acidemia
2-Methylbutyryl-CoA dehydrogenase deficiency
Methylmalonic acidemia
Health
Rare diseases
Genetic genealogy

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

Add to Reading List

Source URL: www.health.mo.gov

Download Document from Source Website

File Size: 18,33 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