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Jiabao Ren
Jiabao Ren
Hebei Medical University
Sanger sequencing
Gene
Mutation
Medicine
Missense mutation
3
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2
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Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasia.
2021
Medicine
Liyuan Yang
Genqi Lu
Wenjing Shen
Wenjing Chen
Haiyan Lu
Guozhong Zhang
Shuo Yuan
Shushen Zheng
Jiabao Ren
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A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.
2021
Molecular Genetics & Genomic Medicine
Hongyu Zhang
Xuanting Kong
Jiabao Ren
Shuo Yuan
Chunyan Liu
Yan Hou
Ye Liu
Lingqiang Meng
Guozhong Zhang
Qingqing Du
Wenjing Shen
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A novel EDA1 missense mutation in X-linked hypohidrotic ectodermal dysplasia.
2020
Medicine
Xu Wang
Zhiyu Zhang
Shuo Yuan
Jiabao Ren
Hong Qu
Guozhong Zhang
Wenjing Chen
Shushen Zheng
Lingqiang Meng
Jiuping Bai
Qingqing Du
Dongru Yang
Wenjing Shen
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Citations (2)
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