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科研机构
中国医学科学院 北京... [3]
安徽大学 [2]
湖南大学 [2]
复旦大学上海医学院 [1]
内容类型
期刊论文 [8]
发表日期
2019 [8]
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TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
期刊论文
GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 7
作者:
Liu, Jiaqi
;
Wu, Nan
;
Yang, Nan
;
Takeda, Kazuki
;
Chen, Weisheng
收藏
  |  
浏览/下载:63/0
  |  
提交时间:2019/12/05
congenital scoliosis (CS)
16p11.2/TBX6
compound inheritance model
genotype-phenotype correlation
gene dosage
Uniform boundary estimates in homogenization of higher-order elliptic systems
期刊论文
Annali di Matematica Pura ed Applicata (1923 -), 2019, 卷号: Vol.198 No.1, 页码: 97-128
作者:
Weisheng Niu
;
Yao Xu
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/04/24
Elliptic systems
Homogenization
Uniform estimates
Convergence rate
A refined convergence result in homogenization of second order parabolic systems
期刊论文
Journal of Differential Equations, 2019, 卷号: Vol.266 No.12, 页码: 8294-8319
作者:
Weisheng Niu
;
Yao Xu
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  |  
浏览/下载:4/0
  |  
提交时间:2019/04/24
Periodic homogenization
Convergence rates
Time-dependent parabolic systems
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.
期刊论文
Genetics in medicine : official journal of the American College of Medical Genetics, 2019
作者:
Jiaqi Liu
;
Nan Wu
;
Nan Yang
;
Kazuki Takeda
;
Weisheng Chen
收藏
  |  
浏览/下载:48/0
  |  
提交时间:2019/12/13
16p11.2/TBX6
compound
inheritance
model
congenital
scoliosis
(CS)
gene
dosage
genotype-phenotype
correlation
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
期刊论文
Genetics in Medicine, 2019
作者:
Jiaqi Liu
;
Nan Wu
;
Deciphering Disorders Involving Scoliosis and COmorbidities study, Nan Yang
;
Kazuki Takeda
;
Weisheng Chen
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  |  
浏览/下载:40/0
  |  
提交时间:2019/12/13
Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese family
期刊论文
2019
作者:
Ding Xinghuan
;
Zhao Sen
;
Zhang Qianqian
;
Yan Zihui
;
Wang Yang
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2020/01/03
Aneurysm
Genetic
Hemorrhage
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population
期刊论文
2019, 卷号: 688, 页码: 215-220
作者:
Liu, Gang
;
Liu, Sen
;
Li, Xiaoxin
;
Chen, Jia
;
Chen, Weisheng
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/03
Adolescent idiopathic scoliosis (AIS)
PAX1
Northern Han Chinese
Single nucleotide polymorphism (SNP)
PUMC classification system
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
期刊论文
2019, 卷号: 21, 期号: 7, 页码: 1548-1558
作者:
Liu, Jiaqi
;
Wu, Nan
;
Yang, Nan
;
Takeda, Kazuki
;
Chen, Weisheng
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2020/01/03
congenital scoliosis (CS)
16p11.2/TBX6
compound inheritance model
genotype-phenotype correlation
gene dosage
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