aos
Publiée par EDP Santé
Open Access
Numéro
Actual. Odonto-Stomatol.
Numéro 247, Septembre 2009
Page(s) 241 - 254
Section Pathologie
DOI https://doi.org/10.1051/aos/2009016
Publié en ligne 4 septembre 2009
  1. Dann JJ, Crump P, Ringenberg QM. Vertical maxillary deficiency with cleidocranial dysplasia. Diagnostic findings and surgical-orthodontic correction. Am J Orthod 1980;78(5):564-573.
  2. Kohavi D, Becker A, Zilberman Y. Surgical exposure, orthodontic movement, and final tooth position as factors in periodontal breakdown of treated palatally impacted canines. Am J Orthod 1984;85(1):72-77. [CrossRef] [PubMed]
  3. Jensen BL, Kreiborg S. Development of the dentition in cleidocranial dysplasia. J Oral Pathol Med 1990;19:89-93. [CrossRef] [PubMed]
  4. Jensen BL, Kreiborg S. Dental treatment strategies in cleidocranial dysplasia. Br Dent J 1992;172:243-247. [CrossRef] [PubMed]
  5. Chitayat D, Hodkinson,Azouz EM, et al. Intrafamilial variability in cleidocranial dysplasia: A three generation family. Am J Med Genet 1992;42:298-303. [CrossRef]
  6. Jensen BL, Kreiborg S. Craniofacial abnormalities in 52 school-age and adult patients with cleidocranial dysplasia. J Craniofac Genet Dev Biol 1993;14:98-108.
  7. Nienhaus H, Mau U, Zang KD, et al. Pericentric inversion of chromosome 6 in a patient with cleidocranial dysplasia. Am J Med Genet 1993;46:630-631. [CrossRef]
  8. Becker A, Lustmann J, Shteyer A. Cleidocranial dysplasia: Part 1 - General principles of the orthodontic and surgical treatment modality. Am J of Orthod Dentofa Orthop 1997;111(1):28-33. [CrossRef]
  9. Becker A, Shteyer A, Bimstein E, et al. Cleidocranial dysplasia: Part 2 - Treatment protocol for the orthodontic and surgical modality. Am J of Orthod and Dentofa Orthop 1997;111(2):173-183. [CrossRef]
  10. Ducy P, Starbuck M, Priemel M, et al. A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development. Genes Development 1999;13(8):1025-1036. [CrossRef]
  11. Cooper SC, Flaitz CM, Johnston DA, et al. A natural history of cleidocranial dysplasia. Am J Med Genet 2001;104(1):1-6. [CrossRef] [PubMed]
  12. Yoshida T, Kanegane H, Osato M, et al. Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations. Am J Hum Genet 2002;71(4):724-738. [CrossRef] [PubMed]
  13. Libersa P, Rozé D, Libersa C, et al. Hyperodontie et dysplasie cléido crânienne. À propos d'un cas. J dent Québec 2003;40:125-129.
  14. Coffman JA. Runx transcription factors and the developmental balance between cell proliferation and differenciation. Cell Biology International 2003;27:315-324. [CrossRef] [PubMed]
  15. Cohen MM. Craniofacial anomalies: clinical and molecular perspectives. Ann Acad Med Singapore 2003;32:244-251. [PubMed]
  16. Visoky AM, Johnson J, Binga B, et al. Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings. Laryngoscope 2003;113(9):1508-1514. [CrossRef] [PubMed]
  17. Chen S, Santos L, Wu Y et al. Altered gene expression in human cleidocranial dysplasia dental pulp cells. Arch Oral Biol 2005;50(2):227-36. [CrossRef] [PubMed]
  18. Golan I, Waldeck A, Baumert U. Anomalies of the skull in cleidocranial dysplasia. An otorhinolaryngological and craniofacial radiological study. HNO 2004;52(12):1061-1066.

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.