First Page | Document Content | |
---|---|---|
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 findingsAdd to Reading ListSource URL: www.hrsa.govDownload Document from Source WebsiteFile Size: 466,60 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 |