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

Ижил төстэй зүйлс

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