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American Journal of Cancer Research
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December 23, 2015
Genetic polymorphisms in apoptosis-related genes and the prognosis of hepatocellular carcinoma
Guo-Peng Yu, Qian-Yi Xiao, Zhu-Qing Shi, et al.
Genome Medicine
|
October 29, 2022
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses
Fang Fu, Ru Li, Qiuxia Yu, et al.
Stroke and Vascular Neurology
|
August 19, 2022
Temporal trends and rural-urban disparities in cerebrovascular risk factors, in-hospital management and outcomes in ischaemic strokes in China from 2005 to 2015: a nationwide serial cross-sectional survey
Chun-Juan Wang, Hong-Qiu Gu, Xin-Miao Zhang, et al.
Brain : a Journal of Neurology
|
June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease
Shun-Chang Sun, Di Ma, Mei-Yi Li, et al.
Clinical and Translational Medicine
|
June 2, 2023
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism
Na He, Bao-Zhu Guan, Jie Wang, et al.
Nature Genetics
|
June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsy
Henrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Brain : a Journal of Neurology
|
April 1, 2021
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population
Yu-Wen Zhao, Hong-Xu Pan, Qian Zeng, et al.
Brain : a Journal of Neurology
|
December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor
Qi-Ying Sun, Qian Xu, Yun Tian, et al.
Nature Communications
|
May 26, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project
Pei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, et al.
Human Molecular Genetics
|
January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene
Xiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
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of 45
Search research articles
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Showing results (411-420 of 449) with videos related to
Sort By:
Page
of 45
American Journal of Cancer Research
|
December 23, 2015
Genetic polymorphisms in apoptosis-related genes and the prognosis of hepatocellular carcinoma
Guo-Peng Yu, Qian-Yi Xiao, Zhu-Qing Shi, et al.
Genome Medicine
|
October 29, 2022
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses
Fang Fu, Ru Li, Qiuxia Yu, et al.
Stroke and Vascular Neurology
|
August 19, 2022
Temporal trends and rural-urban disparities in cerebrovascular risk factors, in-hospital management and outcomes in ischaemic strokes in China from 2005 to 2015: a nationwide serial cross-sectional survey
Chun-Juan Wang, Hong-Qiu Gu, Xin-Miao Zhang, et al.
Brain : a Journal of Neurology
|
June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease
Shun-Chang Sun, Di Ma, Mei-Yi Li, et al.
Clinical and Translational Medicine
|
June 2, 2023
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism
Na He, Bao-Zhu Guan, Jie Wang, et al.
Nature Genetics
|
June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsy
Henrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Brain : a Journal of Neurology
|
April 1, 2021
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population
Yu-Wen Zhao, Hong-Xu Pan, Qian Zeng, et al.
Brain : a Journal of Neurology
|
December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor
Qi-Ying Sun, Qian Xu, Yun Tian, et al.
Nature Communications
|
May 26, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project
Pei-Kuan Cong, Wei-Yang Bai, Jin-Chen Li, et al.
Human Molecular Genetics
|
January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene
Xiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Page
of 45