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Showing results (231-240 of 236) with videos related to

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American Journal of Human Genetics|June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersYun Tian, Jun-Ling Wang, Wen Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy StudyChang-Qing Gao, Shan-Ni Wang, Mei-Mei Wang, et al.
Nature Communications|December 31, 2024
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populationsMeng-Yuan Yang, Jia-Dong Zhong, Xin Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in <i>NUS1</i> contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample StudyWo-Tu Tian, Fei-Xia Zhan, Zhen-Hua Liu, et al.
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Showing results (231-240 of 236) with videos related to

Sort By:
Pageof 24
You have reached the last page of results.This site can display upto 236 results.
American Journal of Human Genetics|June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersYun Tian, Jun-Ling Wang, Wen Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy StudyChang-Qing Gao, Shan-Ni Wang, Mei-Mei Wang, et al.
Nature Communications|December 31, 2024
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populationsMeng-Yuan Yang, Jia-Dong Zhong, Xin Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in <i>NUS1</i> contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample StudyWo-Tu Tian, Fei-Xia Zhan, Zhen-Hua Liu, et al.
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