| 1 | CRS11, FGFR2 |
| Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutation. | |
| Okajima K, et al. | |
| Am J Med Genet 85(2):160-70 1999 | |
| 2 | ACS1, ACS3, CRS10, CRS11, DEL7P21, CRS5A, CRS5B, CRS6, CRS7B, CRS8, BSCGS1, CRSCNS, FGFR1, FGFR2, FGFR3, MSX2, SADDAN, TWIST1 |
| Craniosynostosis Syndromes: From Genes to Premature Fusion of Skull Bones. | |
| Hehr U, et al. | |
| Mol Genet Metab 68(2):139-151. No abstract available 1999 | |