A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia

Pan, YH; Lu, WY; Meng, WD; Liao, WX; Hu, AQ; Wu, BL; Xiong, F

Xiong, F (通讯作者)，Southern Med Univ, Sch Basic Med Sci, Dept Med Genet, 1838 Guangzhou North Ave, Guangzhou 510515, Peoples R China.

EUROPEAN JOURNAL OF ORAL SCIENCES, 2023; 131 (1):

Abstract

Cleidocranial dysplasia (CCD) is a rare, autosomal dominant hereditary disorder characterized by skeletal malformations and dental abnormalities. The ......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索