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42. Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations. Cunningham ML, Seto ML, Hing AV, Bull MJ, Hopkin RJ, Leppig KA. Birth Defects Res A Clin Mol Teratol; 2006 Feb; 76(2):78-85. PubMed ID: 16463420 [Abstract] [Full Text] [Related]
43. [Pierre Marie-Sainton cleidocranial dysplasia]. Diaconescu S, Păduraru G, Vâscu AM, Burlea M. Rev Med Chir Soc Med Nat Iasi; 2011 Feb; 115(2):341-8. PubMed ID: 21870721 [Abstract] [Full Text] [Related]
44. [Cleidocranial dysplasia. Description and analysis of a patient cohort]. Baumert U, Golan I, Driemel O, Reichert TE, Reicheneder C, Muessig D, Rose E. Mund Kiefer Gesichtschir; 2006 Nov; 10(6):385-93. PubMed ID: 17051365 [Abstract] [Full Text] [Related]
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47. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation. Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama K. Orthod Craniofac Res; 2007 Nov; 10(4):222-5. PubMed ID: 17973689 [Abstract] [Full Text] [Related]
53. Cleidocranial dysplasia in a mother and her daughter within the scope of neurosurgery. Report of two cases. Tokuc G, Boran P, Boran BO. J Neurosurg; 2006 Apr; 104(4 Suppl):290-2. PubMed ID: 16619644 [Abstract] [Full Text] [Related]