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Pan, Y. et al. (2023). A novel single‐base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. European journal of oral sciences. p. n/a. [Online].
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Pan, Y. et al. (2023). A novel single‐base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. European journal of oral sciences. p. n/a. [Online].