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Somatic FGFR and TWIST Mutations are not a Common Cause of Isolated Nonsyndromic Single Suture Craniosynostosis

  • Published:2007-03 Issue:2 Volume:18 Page:312-314
  • ISSN:1049-2275
  • Container-title:Journal of Craniofacial Surgery
  • language:en
  • Short-container-title:

Author:

Anderson Peter J.,Cox Timothy C.,Roscioli Tony,Elakis George,Smithers Lisa,David David J.,Powell Barry

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference11 articles.

1. Apert syndrome results from localised mutations in FGFR2 and is allelic with Crouzon syndrome.;Wilkie;Nature Genet,1995

2. Identical mutations in the FGFR2 gene causes both Pfeiffer and Crouzon syndrome phenotypes.;Rutland;Nature Genet,1995

3. Mutations in the fibroblastic growth factor receptor type 2 gene cause Crouzon syndrome.;Reardon;Nature Genet,1994

4. Mutations in TWIST gene in Saethre-Chotzen Syndrome.;el Ghouzzi;Nature Genet,1997

5. Familail Scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.;Mc Gillivray;J Med Genet,2005

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