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C. Y. Fang, Xue, J. J., Tan, L., Jiang, C. H., Gao, Q. P., Liang, D. S., and Wu, L. Q., A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia, vol. 10, pp. 3539-3544, 2011.
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