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Yufei Xu

Showing results (41-50 of 92) with videos related to

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Genes|November 14, 2019
Clinical Presentation and Novel Pathogenic Variants among 68 Chinese Neurofibromatosis 1 ChildrenRuen Yao, Tingting Yu, Yufei Xu, et al.
Molecular Genetics & Genomic Medicine|October 19, 2020
TRPS1 mutation detection in Chinese patients with Tricho-rhino-phalangeal syndrome and identification of four novel mutationsChen Wang, Yufei Xu, Yanrong Qing, et al.
BMC Pediatrics|February 19, 2024
Sex-specific difference in phenotype of Kabuki syndrome type 2 patients: a matched case-control studyYirou Wang, Yufei Xu, Yao Chen, et al.
Journal of Molecular Neuroscience : MN|January 17, 2020
Clinical and Molecular Characterization of Three Novel ARHGEF9 Mutations in Patients with Developmental Delay and EpilepsyRuen Yao, Yi Zhang, Jie Liu, et al.
Retina (Philadelphia, Pa.)|April 12, 2021
RETINAL AND CHOROIDAL BLOOD PERFUSION IN PATIENTS WITH BIETTI CRYSTALLINE DYSTROPHYYufei Xu, Zuoxin Qin, Nan Wu, et al.
ACS Applied Materials & Interfaces|September 28, 2022
Applications of Functional DNA Materials in Immunomodulatory TherapyYanfei Qu, Fengyun Shen, Ziyi Zhang, et al.
Endocrine Connections|July 26, 2023
Clinical characteristics and genetic expansion of 46,XY disorders of sex development children in a Chinese prospective studyYijun Tang, Yao Chen, Jiayi Wang, et al.
Translational Pediatrics|May 13, 2022
Study of novel <i>NARS2</i> variants in patient of combined oxidative phosphorylation deficiency 24Yi Zhang, Xiangyue Zhao, Yufei Xu, et al.
European Journal of Medical Genetics|May 1, 2018
Compound heterozygous variants of the COG6 gene in a Chinese patient with deficiency of subunit 6 of the conserved oligomeric Golgi complex (COG6-CDG)Guoqiang Li, Yufei Xu, Xuyun Hu, et al.
Journal of Clinical Nursing|May 15, 2023
Bedside nurses' antimicrobial stewardship practice scope and competencies in acute hospital settings: A scoping reviewWenting Zhao, Wei Guo, Pei Sun, et al.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
Genes|November 14, 2019
Clinical Presentation and Novel Pathogenic Variants among 68 Chinese Neurofibromatosis 1 ChildrenRuen Yao, Tingting Yu, Yufei Xu, et al.
Molecular Genetics & Genomic Medicine|October 19, 2020
TRPS1 mutation detection in Chinese patients with Tricho-rhino-phalangeal syndrome and identification of four novel mutationsChen Wang, Yufei Xu, Yanrong Qing, et al.
BMC Pediatrics|February 19, 2024
Sex-specific difference in phenotype of Kabuki syndrome type 2 patients: a matched case-control studyYirou Wang, Yufei Xu, Yao Chen, et al.
Journal of Molecular Neuroscience : MN|January 17, 2020
Clinical and Molecular Characterization of Three Novel ARHGEF9 Mutations in Patients with Developmental Delay and EpilepsyRuen Yao, Yi Zhang, Jie Liu, et al.
Retina (Philadelphia, Pa.)|April 12, 2021
RETINAL AND CHOROIDAL BLOOD PERFUSION IN PATIENTS WITH BIETTI CRYSTALLINE DYSTROPHYYufei Xu, Zuoxin Qin, Nan Wu, et al.
ACS Applied Materials & Interfaces|September 28, 2022
Applications of Functional DNA Materials in Immunomodulatory TherapyYanfei Qu, Fengyun Shen, Ziyi Zhang, et al.
Endocrine Connections|July 26, 2023
Clinical characteristics and genetic expansion of 46,XY disorders of sex development children in a Chinese prospective studyYijun Tang, Yao Chen, Jiayi Wang, et al.
Translational Pediatrics|May 13, 2022
Study of novel <i>NARS2</i> variants in patient of combined oxidative phosphorylation deficiency 24Yi Zhang, Xiangyue Zhao, Yufei Xu, et al.
European Journal of Medical Genetics|May 1, 2018
Compound heterozygous variants of the COG6 gene in a Chinese patient with deficiency of subunit 6 of the conserved oligomeric Golgi complex (COG6-CDG)Guoqiang Li, Yufei Xu, Xuyun Hu, et al.
Journal of Clinical Nursing|May 15, 2023
Bedside nurses' antimicrobial stewardship practice scope and competencies in acute hospital settings: A scoping reviewWenting Zhao, Wei Guo, Pei Sun, et al.
Pageof 10