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[期刊论文] 作者：Xue Gao,Pu Dai,
来源：中华耳科学杂志：英文版 年份：2014
Hearing loss is one of the most common birth defects,with inherited genetic defects play an important role,contributing to about 60%of deafness occurring in inf...
[会议论文] 作者：Pu DAI,Chaochan CAI,Aiting CHEN,Dongyi HAN,
来源：The 4th East Asian Symposium on Otology(第四届东亚耳科研讨会) 年份：2014
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[会议论文] 作者：Guo-jian WANG,Guan-bin ZHANG,Yong-yi YUAN,Sha-sha HUANG,Yuan-Yuan LI,Dong-yang KANG,Jing CHENG,Pu DAI,
来源：The 4th East Asian Symposium on Otology(第四届东亚耳科研讨会) 年份：2014
Objectives: To verify the clinical validity and accuracy of DNA microarray kit for genetic testing of 15 target deafness mutations.Methods: The whole blood samples from 420 outpatients or inpatients w...
Homozygosity Mapping and Whole Exome Sequencing Identify Mutation in TMEM132E gene causing Nonsyndro
[会议论文] 作者：Gong,Qiji Liu,Xiaohan Zhao,Qian Xin,Shan Shan,Baichun Jiang,Rongfang Qiu,Hailing Zhao,Huijun Yuan,Pu Dai,
来源：中华医学会2012年医学遗传学年会暨全国第十一次医学遗传学学术会议 年份：2012
In this report,we identified a homozygous missense mutation in a novel gene,TMEM132E (transmembrane protein 132E),in a chinese consanguineous family with nonsyndromic hearing loss using whole exome se...
[会议论文] 作者：Shiming Yang,Jianan Li,Pu Dai,Weiju Han,Jun Liu,Hui Zhao,Yihui Zouzou,Zhaohui Hou,Qingshan Jiao,Li Sun,
来源：The 4th East Asian Symposium on Otology(第四届东亚耳科研讨会) 年份：2014
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