Cleidocranial dysplasia complicated with congenital coxa vara: report of one case

WANG De-hua; LAN Jun; XIAO Gang

Journal of China Clinic Medical Imaging ›› 2016, Vol. 27 ›› Issue (5) : 379-380.

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WANG De-hua, LAN Jun, XIAO Gang. Cleidocranial dysplasia complicated with congenital coxa vara: report of one case[J]. Journal of China Clinic Medical Imaging. 2016, 27(5): 379-380

References

[1]陈志军，邱勇，孙旭，等. 颅锁骨发育不全伴脊柱侧凸一例报告[J]. 中华骨科杂志，2008，28（9）：781－782.
[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.