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HARVARD Citation
Zeng, L. et al. (2018). A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia. Archives of oral biology. pp. 243-248. [Online].
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Zeng, L. et al. (2018). A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia. Archives of oral biology. pp. 243-248. [Online].