Heterozygous P250L mutation of fibroblast growth factor receptor 3 in a case of isolated craniosynostosis

Lignende værker

• Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
  af: Hughes, J., et al.
  Udgivet: (2001)
• Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.
  af: Golla, A, et al.
  Udgivet: (1997)
• Medical genetics: advances in brief: Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis
  af: Barnicoat, Angela
  Udgivet: (1998)
• Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice
  af: Vissers, Lisenka E. L. M., et al.
  Udgivet: (2011)
• Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population
  af: Pandey, Rajeev Kumar, et al.
  Udgivet: (2013)