2 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 18701883 | Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3). | 2009 Jan | 1 |
| 2 | 16263090 | Fibroblast growth factor 3, a protein with a dual subcellular fate, is interacting with human ribosomal protein S2. | 2005 Dec 16 | 1 |