Atypical Crouzon Syndrome With a Novel Cys62Arg Mutation in FGFR2 Presenting With Sagittal Synostosis.

समान संसाधन

• FGFR2 Mutation p.Cys342Arg Enhances Mitochondrial Metabolism-Mediated Osteogenesis via FGF/FGFR-AMPK-Erk1/2 Axis in Crouzon Syndrome
  द्वारा: Yidi Wang, और अन्य
  प्रकाशित: (2022-10-01)
• Apparently synonymous substitutions in FGFR2affect splicing and result in mild Crouzon syndrome
  द्वारा: Fenwick, A, और अन्य
  प्रकाशित: (2014)
• Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: Implications for genetic testing in "paternal age-effect" syndromes.
  द्वारा: Goriely, A, और अन्य
  प्रकाशित: (2010)
• A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome.
  द्वारा: de Ravel, T, और अन्य
  प्रकाशित: (2005)
• Implications of a vertex bulge following modified strip craniectomy for sagittal synostosis.
  द्वारा: Marucci, D, और अन्य
  प्रकाशित: (2008)