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	Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia
	Tingting Zhang; Jing Wu; Xiaoxue Zhao; Feifei Hou; Tengfei Ma; Huijuan Wang; Xu Zhang; Xiangyu Zhang
刊名	Archives of Oral Biology
	2019
卷号	Vol.100页码:49-56
关键词	Cleidocranial dysplasia RUNX2 Splice-site mutation Whole-exome sequencing IBSP
ISSN号	0003-9969
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/4735741
专题	湖南大学
作者单位	1.a Department of Oral and Maxillofacial Surgery, Stomatological Hospital of Tianjin Medical University, Tianjin 300070, China 2.School and Hospital of Stomatology, Tianjin Medical University, 12 Qixiangtai Road, Tianjin 300070, China 3.Department of Pediatric Dentistry, Stomatological Hospital of Tianjin Medical University, Tianjin 300070, China
推荐引用方式 GB/T 7714	Tingting Zhang,Jing Wu,Xiaoxue Zhao,et al. Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia[J]. Archives of Oral Biology,2019,Vol.100:49-56.
APA	Tingting Zhang.,Jing Wu.,Xiaoxue Zhao.,Feifei Hou.,Tengfei Ma.,...&Xiangyu Zhang.(2019).Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia.Archives of Oral Biology,Vol.100,49-56.
MLA	Tingting Zhang,et al."Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia".Archives of Oral Biology Vol.100(2019):49-56.

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