Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.

Ítems similars

• Medical genetics: advances in brief: Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis
  per: Barnicoat, Angela
  Publicat: (1998)
• Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis.
  per: Reardon, W, et al.
  Publicat: (1997)
• Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.
  per: Golla, A, et al.
  Publicat: (1997)
• Heterozygous P250L mutation of fibroblast growth factor receptor 3 in a case of isolated craniosynostosis
  per: Schindler, S, et al.
  Publicat: (2002)
• Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population
  per: Pandey, Rajeev Kumar, et al.
  Publicat: (2013)