1. A novel single‐base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. (4th January 2023) Authors: Pan, Yuhua; Lu, Wanyu; Meng, Weidong; Liao, Wenxiao; Hu, Aiqin; Wu, Buling; Xiong, Fu Journal: European journal of oral sciences Issue: Volume 131:Number 1(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗