First Page | Document Content | |
---|---|---|
Date: 2013-08-28 08:18:01Pediatrics Rare diseases Channelopathy Cystic fibrosis Proband Meconium Family history Genetic testing Sweat test Health Medicine Genetics | Cystic Fibrosis Genetic Testing Interpretation Order FormAdd to Reading ListSource URL: www.asperbio.comDownload Document from Source WebsiteFile Size: 78,50 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 |