Full text
PDF



Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bellus G. A., Gaudenz K., Zackai E. H., Clarke L. A., Szabo J., Francomano C. A., Muenke M. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes. Nat Genet. 1996 Oct;14(2):174–176. doi: 10.1038/ng1096-174. [DOI] [PubMed] [Google Scholar]
- Graham J. M., Jr, Braddock S. R., Mortier G. R., Lachman R., Van Dop C., Jabs E. W. Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene. Am J Med Genet. 1998 May 26;77(4):322–329. doi: 10.1002/(sici)1096-8628(19980526)77:4<322::aid-ajmg14>3.0.co;2-k. [DOI] [PubMed] [Google Scholar]
- Moloney D. M., Wall S. A., Ashworth G. J., Oldridge M., Glass I. A., Francomano C. A., Muenke M., Wilkie A. O. Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis. Lancet. 1997 Apr 12;349(9058):1059–1062. doi: 10.1016/s0140-6736(96)09082-4. [DOI] [PubMed] [Google Scholar]
- Reardon W., Wilkes D., Rutland P., Pulleyn L. J., Malcolm S., Dean J. C., Evans R. D., Jones B. M., Hayward R., Hall C. M. Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis. J Med Genet. 1997 Aug;34(8):632–636. doi: 10.1136/jmg.34.8.632. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robin N. H., Scott J. A., Cohen A. R., Goldstein J. A. Nonpenetrance in FGFR3-associated coronal synostosis syndrome. Am J Med Genet. 1998 Nov 16;80(3):296–297. [PubMed] [Google Scholar]

