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山东大学 [13]
复旦大学上海医学院 [13]
中国医学科学院 北... [10]
武汉大学 [6]
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会议论文 [56]
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浏览/检索结果:
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内容类型:会议论文
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Multiple cancer susceptible genes sequencing in BRCA-negative breast cancers with high hereditary risk
会议论文
作者:
Lang, G-T
;
Hu, X.
;
Shao, Z-M
;
Huang, W.
;
Shi, J-X
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/05
germline mutation
BRCA-negative
hereditary breast cancer
multiple-gene sequencing
Detection of ALK and EGFR gene mutation in non-small cell lung adenocarcinoma with brain metastases and its correlation with clinicopathological features
会议论文
作者:
Mao, Luning
;
Xu, Chenyue
;
Xiong, Ji
;
Wang, Yin
;
Wang, Xin
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/12/05
Low Power State Assignments by Quantum-based Genetic Algorithm
会议论文
2018 International Conference on Information Systems and Computer Aided Education, ICISCAE 2018, Changchun, China, 2018-07-06
作者:
Liu, Wenbo
;
He, Anping
;
Zhou, Ning
;
Gao, Xinyan
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/02
Computer aided instruction
Electric power supplies to apparatus
Energy utilization
Genes
Genetic algorithms
Information systems
Information use
Integrated circuit manufacture
Multiobjective optimization
Quantum computers
Quantum theory
State assignment, Circuit designs
Low energy consumption
Low-power circuit
Low-power design
Multi-objective genetic algorithm
Optimal solutions
Quantum Computing
Single gene mutation, Low power electronics
RET Gene, a New Choice for NSCLC
会议论文
作者:
Wang, Y.
;
Ma, K.
;
Xu, Y.
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/05
RET gene mutation
cabozantinib
Targeted therapy
Gene Mutation Profile in Patients with Acquired Pure Red Cell Aplasia
会议论文
BLOOD, 2018-11-29
作者:
Long, Zhangbiao
;
Li, Hongmin
;
Du, Yali
;
Wang, Zhao
;
Han, Bing
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2020/01/03
INTELLECTUAL DISABILITY AND OVER-GROWTH -- A CASE CAUSED BY NOVEL MUTATION OF NFIX GENE BASED ON WHOLE-EXON SEQUENCING
会议论文
作者:
Lu, Wei
;
Wu, Bing-Bing
;
Zhang, Ping
;
Wang, Hui-Jun
;
Yang, Lin
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
Earlier onset age of p.R179 than p.R176 mutation of FGF23 gene in autosomal dominant hypophosphatemic rickets: Analysis of 6 Chinese pedigrees and review of the literature.
会议论文
JOURNAL OF BONE AND MINERAL RESEARCH, 2017-12-01
作者:
Zhao, Zhen
;
Liu, Chang
;
Wang, Ou
;
Li, Mei
;
Xing, Xiaoping
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2020/01/04
A novel mutation in the C10orf2 gene causes Perrault Syndrome with primary ovarian insufficiency
会议论文
33rd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology (ESHRE), JUL 02-05, 2017
作者:
Zhao, S.
;
Li, G.
;
Wang, W.
;
Qin, Y.
;
Chen, Z. J.
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/31
A new heterozygous mutation site of SCN2A gene in a monozygotic twin family with genetic epilepsy with febrile seizures plus(GEFS+) using targeted nextgeneration sequencing
会议论文
第七届CAAE国际癫痫论坛
作者:
Li WN(李文娜)
;
Liu XW(刘学伍)
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/31
SCN
A new heterozygous mutation site of SCN2A gene in a monozygotic twin family with genetic epilepsy with febrile seizures plus
using targeted nextgeneration sequencing
Study on A Class of Genetic Variation Algorithm in Gene Expression
会议论文
Chinese Automation Congress (CAC), OCT 20-22, 2017
作者:
Zhao, Yuqing
;
Gao, Rui
;
Dong, Guiying
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/31
gene mutation
DNA sequence alignment
genetic variation algorithm
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