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Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case

Xue-Yan Qin Pei-Zeng Jia Hua-Xiang Zhao Wei-Ran Li Feng Chen Jiu-Xiang Lin

中华医学杂志（英文版）2017，Vol.130Issue(2)：165-170,6.

中华医学杂志（英文版）2017，Vol.130Issue(2)：165-170,6.DOI:10.4103/0366-6999.197996

Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case

Xue-Yan Qin ¹Pei-Zeng Jia ¹Hua-Xiang Zhao ¹Wei-Ran Li ¹Feng Chen ²Jiu-Xiang Lin¹

作者信息

1. Department of Orthodontics, Peking University School and Hospital of Stomatology, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing 100081, China
2. Central Laboratory, Peking University School and Hospital of Stomatology, National Engineering Laboratory for Digital and Material Technology of Stomatology,Beijing Key Laboratory of Digital Stomatology, Beijing 100081, China
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摘要

关键词

Cleidocranial Dysplasia/Frameshift Mutation/Runt-related Transcription Factor 2

Key words

Cleidocranial Dysplasia/Frameshift Mutation/Runt-related Transcription Factor 2

引用本文复制引用

Xue-Yan Qin,Pei-Zeng Jia,Hua-Xiang Zhao,Wei-Ran Li,Feng Chen,Jiu-Xiang Lin..Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case[J].中华医学杂志（英文版）,2017,130(2):165-170,6.

基金项目

This work was supported by a grant from the Natural Science Foundation of China (No.81200762). （No.81200762）

中华医学杂志（英文版）

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ISSN：0366-6999

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