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	Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review
	Ma, Dan; Wang, Xuxia; Guo, Jun; Zhang, Jun; Cai, Tao
刊名	MEDICINE
	2018
卷号	97期号:32
关键词	cleidocranial dysplasia phenotype-genotype correlation RUNX2 supernumerary teeth
DOI	10.1097/MD.0000000000011328
URL标识	查看原文
公开日期	[db:dc_date_available]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4580044
专题	山东大学
作者单位	1.Shandong Univ, Sch Stomatol, Dept Orthodont, Wenhua West Rd 44-1, Jinan 250012, Shandong, Peoples R China. 2.[Ma, Dan 3.Cai, Tao
推荐引用方式 GB/T 7714	Ma, Dan,Wang, Xuxia,Guo, Jun,et al. Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review[J]. MEDICINE,2018,97(32).
APA	Ma, Dan,Wang, Xuxia,Guo, Jun,Zhang, Jun,&Cai, Tao.(2018).Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review.MEDICINE,97(32).
MLA	Ma, Dan,et al."Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review".MEDICINE 97.32(2018).

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