搜索筛选:
搜索耗时0.0926秒,为你在为你在102,285,761篇论文里面共找到 18 篇相符的论文内容
发布年度:
[期刊论文] 作者：Bofeng LI,Zhetao ZHANG,,
来源：Journal of Geodesy and Geoinformation Science 年份：2019
Time correlations always exist in modern geodetic data,and ignoring these time correlations will affect the precision and reliability of solutions. In this paper,several methods for processing kinemat...
[期刊论文] 作者：LI Zhetao,XIE Jingxiong,ZHU Ge,
来源：城市道桥与防洪 年份：2016
该文从挂篮荷载计算、施工流程、支座及临时固结施工、挂篮安装及试验、合拢段施工、模板制作安装、钢筋安装、混凝土的浇筑及养生、测量监控等方面人手,介绍了S226海滨大桥...
[期刊论文] 作者：LI Xiuxian,LI Zhetao,OUYANG Yan,DUAN Haohua,XIANG Liyao,
来源：中兴通讯技术:英文版 年份：2021
Mobile edge users(MEUs)collect data from sensor devices and report to cloud systems,which can facilitate numerous applications in sensor‑cloud systems(SCS).However,because there is no effective way to access the ground truth to verify the ......
[期刊论文] 作者：TIAN Shujuan,FAN Xiaoping,LI Zhetao,PAN Tian,CHOI Youngjune,SEKIYA Hiroo,,
来源：Chinese Journal of Electronics 年份：2016
An orthogonal-gradient measurement matrix construction algorithm is proposed for reducing the maximum and average mutual-coherence of sensing matrix. It shrinks...
[期刊论文] 作者：PEI Tingrui,LEI Fangqing,LI Zhetao,ZHU Gengming,PENG Xin,Youngjune CHOI,Hiroo SEKIYA,,
来源：Chinese Journal of Electronics 年份：2017
In wireless sensor networks,congestion leads to buffer overflowing,and increases delay.The traditional solutions use rate adjustment to mitigate congestion,thus...
A novel insertion mutation in the ATP7A gene associated with delayed infantile onset of Menkes disea
[会议论文] 作者：Li Wugao,Yan Tizhen,Tang Ning,Li Zhetao,Huang Jiwei,Tan Jianqiang,Pan Lizhen,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
...
[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
...
6p22.3 deletion: report of a boy with severe intellectual disability, autism, and electroencephalogr
[会议论文] 作者：Yan Tizhen,Zeng Ting,Wei Xiao-nin,Ding Yan-ling,Li Wugao,Li Zhetao,Weo Shuo-feng,Luo Shi-qiang,Cai Ren,
来源：第十四次全国医学遗传学学术会议 年份：2015
The interstitial deletions involving the 6p22-p24 chromosomal region are characterized by variable phenotype, according to the different size of the deleted regions and the small amount of patients re...
[会议论文] 作者：Yan Tizhen,Li Wugao,Tang Xiangrong,Li Zhetao,Wang Lin,Mo Lian,Huang Jiwei,Yang Yan,Cai Ren,Tang Ning,
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
...
Whole-exome sequencing identifies two novel MARVELD2 frame-shift mutations as a cause of autosomal r
[会议论文] 作者：Yan Tizhen,Tang Ning,Li Wugao,Li Zhetao,Luo Shiqiang,Li Jingwen,Cai Ren,Tang Xiangrong,Yang Yan,Wang,
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
Background The genetic heterogeneity of hearing loss makes genetic diagnosis expensive and time consuming using available methods....
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...
Targeted genomic capture and massively parallel sequencing of a Chinese family with non-syndromic lo
[会议论文] 作者：Yan Tizhen,Tang Xiangrong,Zeng Dingyuan,Li Wugao,Li Zhetao,Luo Shiqiang,Yang Yan,Li Jingwen,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
Background Wolfram syndrome gene 1 (WFS1) accounts for most of the familial non-syndromic low-frequency sensorineural hearing loss (LFSNHL) which is characterized by an unusual type of hearing loss in...
Whole-exome sequencing identifies two novel MARVELD2 frame-shift mutations as a cause of autosomal r
[会议论文] 作者：Yan Tizhen,Tang Ning,Li Wugao,Li Zhetao,Tang Xiangrong,Luo Shiqiang,Yang Yan,Li Jingwen,Wang Lin,Zeng,
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
Background The genetic heterogeneity of hearing loss makes genetic diagnosis expensive and time consuming using available methods....
[会议论文] 作者：Tizhen,Tan Jian-qiang,Tang Ning,Cai Ren,Zeng Dingyuan,Luo Shi-qiang,Ya Jiaolian,Pan Lizhen,Li Wugao,Li Zhetao,
来源：第十四次全国医学遗传学学术会议 年份：2015
Background: The human X chromosome carries regions prone to genomic instability:the Xq27.3 unstable region, containing the (CGG) n repeat expansion in the FMR1 gene is associated with fragile X syndro...
Detection of rare alpha-thalassemia by using multiplex ligation-dependent probe amplification in sou
[会议论文] 作者：Cai Ren,Tang Ning,Huang Jiwei,Yan Tizhen,Luo Shiqiang,Li Wugao,Li Zhetao,Huang Jun,Li Jingwen,Zhong qingyan,
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
...
[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
...
Whole-exome sequencing identifies two novel MARVELD2 frame-shift mutations as a cause of autosomal r
[会议论文] 作者：Yan Tizhen,Cai Ren,Tang Ning,Li Wugao,Li Zhetao,Tang Xiangrong,Luo Shiqiang,Yang Yan,Li Ji ngwen,Wang,
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
...
相关搜索：
