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| Cleidocranial dysplasia complicated with congenital coxa vara: report of one case |
| Department of Radiology, Xiaogan Central Hospital, Xiaogan Hubei 432000, China |
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[2]Kamamoto M, Machida J, Miyachi H, et al. A novel mutation in the C-terminal region of RUNX2/CBFA1 distal to the DNA-binding runt domain in a Japanese patient with cleidocranial dysplasia[J]. Int J Oral Maxillofac Surg, 2011, 10(4): 434-437.
[3]Zhang C, Zheng S, Wang Y, et al. Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia[J]. Mutagenesis, 2010, 25(6): 589-594.
[4]Mundlos S. Cleidocranial dysplasia: Clinical and molecular genetics[J]. J Med Genet, 1999, 36(3): 177-182. |
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2016, Vol. 27 
