Similar articles for PMID: 9950359

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1

Lajeunie E, El Ghouzzi V, Le Merrer M, Munnich A, Bonaventure J, Renier D. Lajeunie E, et al. J Med Genet. 1999 Jan;36(1):9-13. J Med Genet. 1999. PMID: 9950359 Free PMC article.

2

Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome.

Renier D, El-Ghouzzi V, Bonaventure J, Le Merrer M, Lajeunie E. Renier D, et al. J Neurosurg. 2000 Apr;92(4):631-6. doi: 10.3171/jns.2000.92.4.0631. J Neurosurg. 2000. PMID: 10761652

3

[A case of bilateral coronal craniosynostosis with the P250R mutation in FGFR3 gene].

Mori F, Kuwajima K, Yamanaka K, Kondou I. Mori F, et al. No To Hattatsu. 2001 Jan;33(1):53-7. No To Hattatsu. 2001. PMID: 11197897 Japanese.

4

Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.

Golla A, Lichmer P, von Gernet S, Winterpacht A, Fairley J, Murken J, Schuffenhauer S. Golla A, et al. J Med Genet. 1997 Aug;34(8):683-4. doi: 10.1136/jmg.34.8.683. J Med Genet. 1997. PMID: 9279764 Free PMC article.

5

Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene.

Graham JM Jr, Braddock SR, Mortier GR, Lachman R, Van Dop C, Jabs EW. Graham JM Jr, et al. Am J Med Genet. 1998 May 26;77(4):322-9. doi: 10.1002/(sici)1096-8628(19980526)77:4<322::aid-ajmg14>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9600744

6

[Typical features of craniofacial growth of the FGFR3-associated coronal synostosis syndrome (so-called Muenke craniosynostosis)].

Reinhart E, Eulert S, Bill J, Würzler K, Phan The L, Reuther J. Reinhart E, et al. Mund Kiefer Gesichtschir. 2003 May;7(3):132-7. doi: 10.1007/s10006-002-0447-7. Epub 2003 Apr 30. Mund Kiefer Gesichtschir. 2003. PMID: 12764678 German.

7

Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis.

Moloney DM, Wall SA, Ashworth GJ, Oldridge M, Glass IA, Francomano CA, Muenke M, Wilkie AO. Moloney DM, et al. Lancet. 1997 Apr 12;349(9058):1059-62. doi: 10.1016/s0140-6736(96)09082-4. Lancet. 1997. PMID: 9107244

8

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

Muenke M, Gripp KW, McDonald-McGinn DM, Gaudenz K, Whitaker LA, Bartlett SP, Markowitz RI, Robin NH, Nwokoro N, Mulvihill JJ, Losken HW, Mulliken JB, Guttmacher AE, Wilroy RS, Clarke LA, Hollway G, Adès LC, Haan EA, Mulley JC, Cohen MM Jr, Bellus GA, Francomano CA, Moloney DM, Wall SA, Wilkie AO, et al. Muenke M, et al. Am J Hum Genet. 1997 Mar;60(3):555-64. Am J Hum Genet. 1997. PMID: 9042914 Free PMC article.

9

FGFR3 P250R mutation increases the risk of reoperation in apparent 'nonsyndromic' coronal craniosynostosis.

Thomas GP, Wilkie AO, Richards PG, Wall SA. Thomas GP, et al. J Craniofac Surg. 2005 May;16(3):347-52; discussion 353-4. doi: 10.1097/01.scs.0000157024.56055.f2. J Craniofac Surg. 2005. PMID: 15915095

10

Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.

Lowry RB, Jabs EW, Graham GE, Gerritsen J, Fleming J. Lowry RB, et al. Am J Med Genet. 2001 Nov 22;104(2):112-9. doi: 10.1002/ajmg.10049. Am J Med Genet. 2001. PMID: 11746040

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