First Page | Document Content | |
---|---|---|
![]() Date: 2007-10-17 09:01:33Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Mitochondrial trifunctional protein deficiency Methylcrotonyl-CoA 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy | Add to Reading List |
![]() | 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 |