Similar articles for PMID: 16492963

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1

A cloverleaf skull associated with Crouzon syndrome.

Chen CP, Lin SP, Su YN, Huang JK, Wang W. Chen CP, et al. Arch Dis Child Fetal Neonatal Ed. 2006 Mar;91(2):F98. doi: 10.1136/adc.2005.087577. Arch Dis Child Fetal Neonatal Ed. 2006. PMID: 16492963 Free PMC article. No abstract available.

2

Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome.

Chaisrisawadisuk S, Hammam E, Molloy CJ, Barnett C, Anderson PJ, Moore MH. Chaisrisawadisuk S, et al. J Craniofac Surg. 2021 Jan-Feb 01;32(1):261-264. doi: 10.1097/SCS.0000000000006999. J Craniofac Surg. 2021. PMID: 32956303

3

The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.

Perlyn CA, DeLeon VB, Babbs C, Govier D, Burell L, Darvann T, Kreiborg S, Morriss-Kay G. Perlyn CA, et al. Cleft Palate Craniofac J. 2006 Nov;43(6):740-8. doi: 10.1597/05-212. Cleft Palate Craniofac J. 2006. PMID: 17105336

4

Cloverleaf skull syndrome. Case report.

Muller PJ, Hoffman HJ. Muller PJ, et al. J Neurosurg. 1975 Jul;43(1):86-91. doi: 10.3171/jns.1975.43.1.0086. J Neurosurg. 1975. PMID: 1141987

5

Atypical Crouzon syndrome with a novel Cys62Arg mutation in FGFR2 presenting with sagittal synostosis.

Sharma VP, Wall SA, Lord H, Lester T, Wilkie AO. Sharma VP, et al. Cleft Palate Craniofac J. 2012 May;49(3):373-7. doi: 10.1597/11-185. Epub 2011 Nov 25. Cleft Palate Craniofac J. 2012. PMID: 22117175

6

Radiology of the craniofacial anomalies.

Mafee MF, Valvassori GE. Mafee MF, et al. Otolaryngol Clin North Am. 1981 Nov;14(4):939-88. Otolaryngol Clin North Am. 1981. PMID: 7038590 Review. No abstract available.

7

Sacral appendage in a child with an FGFR2 mutation: a report and review.

Shanske AL, Staffenberg D, Goodrich JT. Shanske AL, et al. Am J Med Genet A. 2008 Aug 15;146A(16):2172-5. doi: 10.1002/ajmg.a.32436. Am J Med Genet A. 2008. PMID: 18629881 No abstract available.

8

Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y).

Olafsdóttir H, Darvann TA, Hermann NV, Oubel E, Ersbøll BK, Frangi AF, Larsen P, Perlyn CA, Morriss-Kay GM, Kreiborg S. Olafsdóttir H, et al. J Anat. 2007 Jul;211(1):37-52. doi: 10.1111/j.1469-7580.2007.00751.x. Epub 2007 Jun 6. J Anat. 2007. PMID: 17553099 Free PMC article.

9

Craniofacial growth in premature craniofacial synostosis.

Kreiborg S, Pruzansky S. Kreiborg S, et al. Scand J Plast Reconstr Surg. 1981;15(3):171-86. doi: 10.3109/02844318109103432. Scand J Plast Reconstr Surg. 1981. PMID: 7347001

10

S267P mutation in FGFR2: first report in a patient with Crouzon syndrome.

Ke R, Yang X, Ge M, Cai T, Lei J, Mu X. Ke R, et al. J Craniofac Surg. 2015 Mar;26(2):592-4. doi: 10.1097/SCS.0000000000001527. J Craniofac Surg. 2015. PMID: 25759927

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