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Molecular Cytogenetics
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March 2, 2019
Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China
Chang Liu, Xiangzhong Zhang, Jicheng Wang, et al.
International Journal of Pediatric Otorhinolaryngology
|
August 8, 2022
Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice
Chang Liu, Yanlin Huang, Yan Zhang, et al.
QJM : Monthly Journal of the Association of Physicians
|
October 11, 2024
Exome sequencing for nonimmune hydrops fetalis and clinical utility of data reanalysis
Chang Liu, Yanlin Huang, Yunan Wang, et al.
Frontiers in Genetics
|
September 26, 2025
Clinical utility of exome sequencing in hearing loss: a retrospective cohort study
Chang Liu, Yanlin Huang, Anpeng Fu, et al.
Journal of Translational Medicine
|
July 9, 2024
High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases
Yimo Zeng, Hongke Ding, Xingwang Wang, et al.
Small Methods
|
October 6, 2023
Diagnosis of Esophageal Squamous Cell Carcinoma by High-Performance Serum Metabolic Fingerprints: A Retrospective Study
Yida Huang, Haijun Yang, Junkuo Li, et al.
Physical Review Letters
|
June 11, 2021
Search for Light Dark Matter-Electron Scattering in the PandaX-II Experiment
Chen Cheng, Pengwei Xie, Abdusalam Abdukerim, et al.
Physical Review Letters
|
May 16, 2022
Search for Cosmic-Ray Boosted Sub-GeV Dark Matter at the PandaX-II Experiment
Xiangyi Cui, Abdusalam Abdukerim, Zihao Bo, et al.
Physical Review Letters
|
January 14, 2022
Dark Matter Search Results from the PandaX-4T Commissioning Run
Yue Meng, Zhou Wang, Yi Tao, et al.
Physical Review Letters
|
October 28, 2022
First Search for the Absorption of Fermionic Dark Matter with the PandaX-4T Experiment
Linhui Gu, Abdusalam Abdukerim, Zihao Bo, et al.
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of 12
Search research articles
Search
Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
Molecular Cytogenetics
|
March 2, 2019
Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China
Chang Liu, Xiangzhong Zhang, Jicheng Wang, et al.
International Journal of Pediatric Otorhinolaryngology
|
August 8, 2022
Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice
Chang Liu, Yanlin Huang, Yan Zhang, et al.
QJM : Monthly Journal of the Association of Physicians
|
October 11, 2024
Exome sequencing for nonimmune hydrops fetalis and clinical utility of data reanalysis
Chang Liu, Yanlin Huang, Yunan Wang, et al.
Frontiers in Genetics
|
September 26, 2025
Clinical utility of exome sequencing in hearing loss: a retrospective cohort study
Chang Liu, Yanlin Huang, Anpeng Fu, et al.
Journal of Translational Medicine
|
July 9, 2024
High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases
Yimo Zeng, Hongke Ding, Xingwang Wang, et al.
Small Methods
|
October 6, 2023
Diagnosis of Esophageal Squamous Cell Carcinoma by High-Performance Serum Metabolic Fingerprints: A Retrospective Study
Yida Huang, Haijun Yang, Junkuo Li, et al.
Physical Review Letters
|
June 11, 2021
Search for Light Dark Matter-Electron Scattering in the PandaX-II Experiment
Chen Cheng, Pengwei Xie, Abdusalam Abdukerim, et al.
Physical Review Letters
|
May 16, 2022
Search for Cosmic-Ray Boosted Sub-GeV Dark Matter at the PandaX-II Experiment
Xiangyi Cui, Abdusalam Abdukerim, Zihao Bo, et al.
Physical Review Letters
|
January 14, 2022
Dark Matter Search Results from the PandaX-4T Commissioning Run
Yue Meng, Zhou Wang, Yi Tao, et al.
Physical Review Letters
|
October 28, 2022
First Search for the Absorption of Fermionic Dark Matter with the PandaX-4T Experiment
Linhui Gu, Abdusalam Abdukerim, Zihao Bo, et al.
Page
of 12