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浏览/检索结果: 共7条，第1-7条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia 期刊论文 Archives of Oral Biology, 2019, 卷号: Vol.100, 页码: 49-56 作者:  Tingting Zhang;  Jing Wu;  Xiaoxue Zhao;  Feifei Hou;  Tengfei Ma 收藏  |  浏览/下载：31/0  |  提交时间：2019/12/17 Cleidocranial  dysplasia  RUNX2  Splice-site  mutation  Whole-exome  sequencing  IBSP   Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia. 期刊论文 Archives of oral biology, 2019, 卷号: Vol.100, 页码: 49-56 作者:  Tingting Zhang;  Jing Wu;  Xiaoxue Zhao;  Feifei Hou;  Tengfei Ma 收藏  |  浏览/下载：15/0  |  提交时间：2019/12/17 Cleidocranial dysplasia  IBSP  RUNX2  Splice-site mutation  Whole-exome sequencing   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 期刊论文 MEDICINE, 2018, 卷号: 97, 期号: 32 作者:  Ma, Dan;  Wang, Xuxia;  Guo, Jun;  Zhang, Jun;  Cai, Tao 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11 cleidocranial dysplasia  phenotype-genotype correlation  RUNX2  supernumerary teeth   A novel gene mutation of Runx2 in cleidocranial dysplasia 期刊论文 JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES, 2017, 卷号: 37, 期号: 5 作者:  Peng, You-jian;  Chen, Qiao-yun;  Fu, Dong-jie;  Liu, Zhi-ming;  Mao, Tian-tian 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/05 cleidocranial dysplasia  RUNX2  genetic testing  mutation   Novel RUNX2 frameshift mutations in Chinese patients with cleidocranial dysplasia 期刊论文 EUROPEAN JOURNAL OF ORAL SCIENCES, 2013, 卷号: 121, 期号: 3 作者:  Huang, Yanyu;  Song, Yaling;  Zhang, Chenzheng;  Chen, Guoxin;  Wang, Shihua 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05 cleidocranial dysplasia  dental abnormalities  frameshift mutation  runt-related transcription factor 2   CHIP promotes Runx2 degradation and negatively regulates osteoblast differentiation 期刊论文 2010, 2010 Li, Xueni; Huang, Mei; Zheng, Huiling; Wang, Yinyin; Ren, Fangli; Shang, Yu; Zhai, Yonggong; Irwin, David M.; Shi, Yuguang; Chen, Di; Chang, Zhijie 收藏  |  浏览/下载：7/0 A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia 期刊论文 GENETICS AND MOLECULAR RESEARCH, 2010, 卷号: 9, 期号: 1, 页码: 41-47 作者:  Wang, G. X.;  Sun, R. P.;  Song, F. L. 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/26 Cleidocranial dysplasia  Mutation  RUNX2  Gene