These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. Effect of cleidocranial dysplasia-related novel mutation of RUNX2 on characteristics of dental pulp cells and tooth development. Xuan D, Sun X, Yan Y, Xie B, Xu P, Zhang J. J Cell Biochem; 2010 Dec 15; 111(6):1473-81. PubMed ID: 20872798 [Abstract] [Full Text] [Related]
9. 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 15; 76(2):78-85. PubMed ID: 16463420 [Abstract] [Full Text] [Related]
10. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients. Bufalino A, Paranaíba LM, Gouvêa AF, Gueiros LA, Martelli-Júnior H, Junior JJ, Lopes MA, Graner E, De Almeida OP, Vargas PA, Coletta RD. Oral Dis; 2012 Mar 15; 18(2):184-90. PubMed ID: 22023169 [Abstract] [Full Text] [Related]
11. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Ott CE, Leschik G, Trotier F, Brueton L, Brunner HG, Brussel W, Guillen-Navarro E, Haase C, Kohlhase J, Kotzot D, Lane A, Lee-Kirsch MA, Morlot S, Simon ME, Steichen-Gersdorf E, Tegay DH, Peters H, Mundlos S, Klopocki E. Hum Mutat; 2010 Aug 15; 31(8):E1587-93. PubMed ID: 20648631 [Abstract] [Full Text] [Related]