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[会议论文] 作者：Zhang Zhetao,Li Bofeng,Shen Yunzhong,
来源：2016国际大地测量与地球动力学学术讨论会 年份：2016
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[期刊论文] 作者：Zhetao LI,Ziwen CHEN,Wei-Shi ZHENG,Sangyoon OH,Kien NGUYEN,
来源：中国科学：信息科学（英文版） 年份：2022
An increasing number of deep learning methods is being applied to quantify the perception of urban environments,study the relationship between urban appearance and resident safety,and improve urban appearance.Most advanced methods extract i......
[期刊论文] 作者：Tingrui PEI,Yafeng DENG,Zhetao LI,Gengming ZHU,Gaofeng PAN,Youngjune CHOI,Hiroo SEKIYA,,
来源：Science China(Information Sciences) 年份：2016
Dear editor,The Carrier Sense Multiple Access with Collision Avoidance(CSMA/CA)hybrid with the resource reservation approach from Time Division Multiple Address...
[会议论文] 作者：Yan Tizhen,Tang Ning,Luo Shiqiang,Huang Jiwei,Tan Jianqiang,Li Zhetao,Li Wugao,Wang Yuanliu,Cai Ren,
来源：中华医学会第十五次全国医学遗传学学术会议、中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会 年份：2016
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Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalasse
[会议论文] 作者：Lingling Hu,Xuan Shang,Sheng Yi,Ren Cai,Zhetao Li,Cuixian Liu,Yidan Liang,Decheng Cai,Feng Zhang,Xiangmin,
来源：The 2nd International Symposium on Erythrocyte Biology(2016第 年份：2016
Copy number variations (CNVs) can cause many genetic disorders and the structure analysis of unknown CNVs is important for clinical diagnosis.The human α-globin gene cluster lies close to the telomere...
Identification and Clinical Implications of Novel MY015A Mutations in a Non-consanguineous Chinese F
[会议论文] 作者：Yan Tizhen,Li Zhetao,Li Wugao,Tang Ning,Li Jingwen,Cai Ren,Tang Xiangrong,Yang Yan,Zheng Pei,Wang Lin,
来源：第十五次中国中西医结合耳鼻咽喉科专业委员会年会 年份：2016
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally manifested with prelingual hearing l...
Identification and Clinical Implications of Novel MY015A Mutations in a Non-consanguineous Chinese F
[会议论文] 作者：Yan Tizhen,Tang Xiangrong,Li Zhetao,Li Wugao,Tang Ning,Wang Lin,Yang Yan,Li Jingwen,Zheng Pei,Cai Ren,
来源：第十五次中国中西医结合耳鼻咽喉科专业委员会年会 年份：2016
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally manifested with prelingual hearing loss and absence of other clinical manifestat...
[会议论文] 作者：Yan Tizhen,Tang Ning,Li Zhetao,Li Wugao,Tang Xiangrong,Wang Lin,Yang Yan,Huang Jiwei,Zheng Pei,Cai Ren,
来源：中华医学会第十五次全国医学遗传学学术会议、中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会 年份：2016
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