Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients.

Míreanna comhchosúla

• Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.
  de réir: Jehee, F, et al.
  Foilsithe / Cruthaithe: (2005)
• Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis.
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  Foilsithe / Cruthaithe: (2004)
• FGFR3 P250R mutation increases the risk of reoperation in apparent 'nonsyndromic' coronal craniosynostosis.
  de réir: Thomas, G, et al.
  Foilsithe / Cruthaithe: (2005)
• Atypical Crouzon Syndrome With a Novel Cys62Arg Mutation in FGFR2 Presenting With Sagittal Synostosis.
  de réir: Sharma, V, et al.
  Foilsithe / Cruthaithe: (2012)
• Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia.
  de réir: Goriely, A, et al.
  Foilsithe / Cruthaithe: (2005)