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Haiming Yuan

Showing results (21-30 of 59) with videos related to

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Molecular Cytogenetics|December 26, 2015
A de novo triplication on 2q22.3 including the entire ZEB2 gene associated with global developmental delay, multiple congenital anomalies and behavioral abnormalitiesHaiming Yuan, Lina Zhang, Mengfan Chen, et al.
Optics Letters|May 19, 2016
Focusing surface plasmon polaritons and detecting Stokes parameters utilizing nanoslits distributed plasmonic lensesFeng Huang, Xiangqian Jiang, Haiming Yuan, et al.
Molecular Cytogenetics|August 4, 2016
A de novo 1.6Mb microdeletion at 19q13.2 in a boy with Diamond-Blackfan anemia, global developmental delay and multiple congenital anomaliesHaiming Yuan, Zhe Meng, Liping Liu, et al.
Molecular Genetics & Genomic Medicine|April 29, 2026
Pedigree and Functional Analysis of Two Cryptic OTC Variants Causing Ornithine Transcarbamylase Deficiency in Two Unrelated Chinese Male PatientsQingming Wang, Huimin Xiao, Fang Zhang, et al.
BMC Medical Genetics|May 8, 2020
Concurrent pathogenic variants in SLC6A1/NOTCH1/PRIMPOL genes in a Chinese patient with myoclonic-atonic epilepsy, mild aortic valve stenosis and high myopiaHaiming Yuan, Qingming Wang, Yufeng Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 22, 2022
[Genetic and clinical analysis of a novel GLB1 gene variant in a Chinese patient with GM1-gangliosidosis]Shuangxi Cheng, Qingming Wang, Aixin Chen, et al.
Optics Express|October 6, 2012
Optical magnetic field enhancement through coupling magnetic plasmons to Tamm plasmonsHai Liu, Xiudong Sun, Fengfeng Yao, et al.
Molecular Genetics & Genomic Medicine|July 25, 2020
Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disordersHaiming Yuan, Huihua Yuan, Qingming Wang, et al.
Nanoscale|March 25, 2025
Broadband and polarization-independent complex amplitude modulation using a single layer dielectric metasurfaceNa Zhang, Fei Wang, Qixuan Min, et al.
Clinical Genetics|April 24, 2023
RNASEH2C c.194G>A is a Chinese-specific founder mutation in three unrelated patients with Aicardi-Goutières syndrome 3Qingming Wang, Ye Han, Xinlong Zhou, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Molecular Cytogenetics|December 26, 2015
A de novo triplication on 2q22.3 including the entire ZEB2 gene associated with global developmental delay, multiple congenital anomalies and behavioral abnormalitiesHaiming Yuan, Lina Zhang, Mengfan Chen, et al.
Optics Letters|May 19, 2016
Focusing surface plasmon polaritons and detecting Stokes parameters utilizing nanoslits distributed plasmonic lensesFeng Huang, Xiangqian Jiang, Haiming Yuan, et al.
Molecular Cytogenetics|August 4, 2016
A de novo 1.6Mb microdeletion at 19q13.2 in a boy with Diamond-Blackfan anemia, global developmental delay and multiple congenital anomaliesHaiming Yuan, Zhe Meng, Liping Liu, et al.
Molecular Genetics & Genomic Medicine|April 29, 2026
Pedigree and Functional Analysis of Two Cryptic OTC Variants Causing Ornithine Transcarbamylase Deficiency in Two Unrelated Chinese Male PatientsQingming Wang, Huimin Xiao, Fang Zhang, et al.
BMC Medical Genetics|May 8, 2020
Concurrent pathogenic variants in SLC6A1/NOTCH1/PRIMPOL genes in a Chinese patient with myoclonic-atonic epilepsy, mild aortic valve stenosis and high myopiaHaiming Yuan, Qingming Wang, Yufeng Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 22, 2022
[Genetic and clinical analysis of a novel GLB1 gene variant in a Chinese patient with GM1-gangliosidosis]Shuangxi Cheng, Qingming Wang, Aixin Chen, et al.
Optics Express|October 6, 2012
Optical magnetic field enhancement through coupling magnetic plasmons to Tamm plasmonsHai Liu, Xiudong Sun, Fengfeng Yao, et al.
Molecular Genetics & Genomic Medicine|July 25, 2020
Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disordersHaiming Yuan, Huihua Yuan, Qingming Wang, et al.
Nanoscale|March 25, 2025
Broadband and polarization-independent complex amplitude modulation using a single layer dielectric metasurfaceNa Zhang, Fei Wang, Qixuan Min, et al.
Clinical Genetics|April 24, 2023
RNASEH2C c.194G>A is a Chinese-specific founder mutation in three unrelated patients with Aicardi-Goutières syndrome 3Qingming Wang, Ye Han, Xinlong Zhou, et al.
Pageof 6