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Heliyon
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August 16, 2024
Pharmacovigilance analysis of orlistat adverse events based on the FDA adverse event reporting system (FAERS) database
Jinfeng Zhu, Mianda Hu, Yingshi Liang, et al.
Journal of Medical Genetics
|
January 31, 2024
Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort
Xiaohong Yan, Jing Wang, Wen Yang, et al.
Journal of Medical Genetics
|
September 17, 2025
Heterozygous <i>TBX2</i> frameshift variants cause a novel syndromic hearing loss with incompletely penetrant nystagmus
Wan Hua, Yanfei Wang, Xiang Li, et al.
Molecular Genetics & Genomic Medicine
|
April 25, 2019
Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss
Xinlei Li, Bo Tan, Xiaoqian Wang, et al.
Genome Medicine
|
December 19, 2023
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss
Sihan Liu, Mingjun Zhong, Yu Huang, et al.
Human Genetics
|
February 19, 2022
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss
Fengxiao Bu, Mingjun Zhong, Qinyi Chen, et al.
National Science Review
|
August 11, 2023
Structure transformation from Sierpiński triangles to chains assisted by gas molecules
Chao Li, Zhen Xu, Yajie Zhang, et al.
Nature Communications
|
March 13, 2021
On-surface preparation of coordinated lanthanide-transition-metal clusters
Jing Liu, Jie Li, Zhen Xu, et al.
Ebiomedicine
|
May 29, 2026
Optimising POU3F4 variant interpretation through gene-specific evidence in X-linked hearing loss
Jia Geng, Yixin Zhao, Yu Huang, et al.
ACS Nano
|
October 8, 2025
Atom and Molecule Migrations between Scanning Tunneling Microscopy Tips and Surfaces
Xin Li, Yifan Wang, Guilin Zhu, et al.
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Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Heliyon
|
August 16, 2024
Pharmacovigilance analysis of orlistat adverse events based on the FDA adverse event reporting system (FAERS) database
Jinfeng Zhu, Mianda Hu, Yingshi Liang, et al.
Journal of Medical Genetics
|
January 31, 2024
Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort
Xiaohong Yan, Jing Wang, Wen Yang, et al.
Journal of Medical Genetics
|
September 17, 2025
Heterozygous <i>TBX2</i> frameshift variants cause a novel syndromic hearing loss with incompletely penetrant nystagmus
Wan Hua, Yanfei Wang, Xiang Li, et al.
Molecular Genetics & Genomic Medicine
|
April 25, 2019
Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss
Xinlei Li, Bo Tan, Xiaoqian Wang, et al.
Genome Medicine
|
December 19, 2023
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss
Sihan Liu, Mingjun Zhong, Yu Huang, et al.
Human Genetics
|
February 19, 2022
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss
Fengxiao Bu, Mingjun Zhong, Qinyi Chen, et al.
National Science Review
|
August 11, 2023
Structure transformation from Sierpiński triangles to chains assisted by gas molecules
Chao Li, Zhen Xu, Yajie Zhang, et al.
Nature Communications
|
March 13, 2021
On-surface preparation of coordinated lanthanide-transition-metal clusters
Jing Liu, Jie Li, Zhen Xu, et al.
Ebiomedicine
|
May 29, 2026
Optimising POU3F4 variant interpretation through gene-specific evidence in X-linked hearing loss
Jia Geng, Yixin Zhao, Yu Huang, et al.
ACS Nano
|
October 8, 2025
Atom and Molecule Migrations between Scanning Tunneling Microscopy Tips and Surfaces
Xin Li, Yifan Wang, Guilin Zhu, et al.
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of 4