| 1 | FGFR3, CATSHL |
| A Novel Mutation in FGFR3 Causes Camptodactyly, Tall Stature, and Hearing Loss (CATSHL) Syndrome. | |
| Toydemir RM, Brassington AE, Bayrak-Toydemir P, Krakowiak PA, Jorde LB, Whitby FG, Longo N, Viskochil DH, Carey JC, Bamshad MJ. | |
| Am J Hum Genet 79(5):935-941. Epub 2006 Sep 26. 2006 | |