First Page | Document Content | |
---|---|---|
Date: 2007-10-17 09:01:06Medical 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 | Microsoft Word - New Hampshire Insert English FINAL.docAdd to Reading ListSource URL: nergg.orgDownload Document from Source WebsiteFile Size: 11,70 KBShare Document on Facebook |
DOCX DocumentDocID: 1wwhs - View Document | |
DOCX DocumentDocID: 1wv76 - View Document | |
PDF DocumentDocID: 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 DISEASESDocID: 1v3AN - View Document |