| 1 | 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 | |
| 2 | CRS8 |
| Localization of craniosynostosis Adelaide type to 4p16. | |
| Hollway GE, et al. | |
| Hum Mol Genet 4 : 681-683. 1995 | |
| 3 | CRS8 |
| Jackson-Weiss syndrome : clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter. | |
| Ads LC, et al. | |
| Am J Med Genet 51 : 121-130. 1994 | |