| 1 | FGF9, SYNS3 |
| Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndrome. | |
| van den Ende JJ, Borra V, Van Hul W. | |
| Clin Dysmorphol 22(1):1-6. doi: 10.1097/MCD.0b013e3283590986. 2013 | |
| 2 | FGF9, SYNS3 |
| Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene. | |
| Wu XL, Gu MM, Huang L, Liu XS, Zhang HX, Ding XY, Xu JQ, Cui B, Wang L, Lu SY, Chen XY, Zhang HG, Huang W, Yuan WT, Yang JM, Gu Q, Fei J, Chen Z, Yuan ZM, Wang ZG. | |
| Am J Hum Genet 85(1):53-63. 2009 | |