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Haiming Yuan

Showing results (31-40 of 59) with videos related to

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European Journal of Medical Genetics|January 8, 2019
Microdeletion and microduplication of 1p36.11p35.3 involving AHDC1 contribute to neurodevelopmental disorderQingming Wang, Xiaoling Huang, Yanhui Liu, et al.
Cytogenetic and Genome Research|June 15, 2016
Paternal Uniparental Disomy of Chromosome 14 with HypospadiasHaiming Yuan, Yingjun Xie, Qian Li, et al.
Molecular Genetics & Genomic Medicine|July 19, 2023
Novel KCNJ16 variants identified in a Chinese patient with hypokalemic metabolic acidosisJianxiong Chen, Youqing Fu, Yan Sun, et al.
Bioresource Technology|September 19, 2024
Directed evolution and metabolic engineering generate an Escherichia coli cell factory for de novo production of 4-hydroxymandelatePeipei Liu, Qianwen Jin, Xuanye Li, et al.
Oral Diseases|November 28, 2022
Activated fibroblasts induce immune escape of TSCC through CCL25/AKT pathwayYiting Li, Ken Lin, Xiaobin Ren, et al.
Scientific Reports|July 9, 2024
Passive imaging through inhomogeneous scattering mediaYaoming Bian, Fei Wang, Haishan Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Chromosomal microarray analysis of 2000 pediatric cases]Haiming Yuan, Junping Zhu, Xiaoyan Deng, et al.
Frontiers in Genetics|June 1, 2022
Three Novel <i>De Novo ZEB2</i> Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic ReviewYouqing Fu, Wanfang Xu, Qingming Wang, et al.
European Journal of Medical Genetics|April 15, 2018
A de novo 921 Kb microdeletion at 11q13.1 including neurexin 2 in a boy with developmental delay, deficits in speech and language without autistic behaviorsHaiming Yuan, Xiaoxiu Li, Qingming Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 27, 2020
[Identification of a de novo MAP2K1 gene variant in an affected patient with Cardio-facio-cutaneous syndrome]Qingming Wang, Pengliang Chen, Qian Peng, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
European Journal of Medical Genetics|January 8, 2019
Microdeletion and microduplication of 1p36.11p35.3 involving AHDC1 contribute to neurodevelopmental disorderQingming Wang, Xiaoling Huang, Yanhui Liu, et al.
Cytogenetic and Genome Research|June 15, 2016
Paternal Uniparental Disomy of Chromosome 14 with HypospadiasHaiming Yuan, Yingjun Xie, Qian Li, et al.
Molecular Genetics & Genomic Medicine|July 19, 2023
Novel KCNJ16 variants identified in a Chinese patient with hypokalemic metabolic acidosisJianxiong Chen, Youqing Fu, Yan Sun, et al.
Bioresource Technology|September 19, 2024
Directed evolution and metabolic engineering generate an Escherichia coli cell factory for de novo production of 4-hydroxymandelatePeipei Liu, Qianwen Jin, Xuanye Li, et al.
Oral Diseases|November 28, 2022
Activated fibroblasts induce immune escape of TSCC through CCL25/AKT pathwayYiting Li, Ken Lin, Xiaobin Ren, et al.
Scientific Reports|July 9, 2024
Passive imaging through inhomogeneous scattering mediaYaoming Bian, Fei Wang, Haishan Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Chromosomal microarray analysis of 2000 pediatric cases]Haiming Yuan, Junping Zhu, Xiaoyan Deng, et al.
Frontiers in Genetics|June 1, 2022
Three Novel <i>De Novo ZEB2</i> Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic ReviewYouqing Fu, Wanfang Xu, Qingming Wang, et al.
European Journal of Medical Genetics|April 15, 2018
A de novo 921 Kb microdeletion at 11q13.1 including neurexin 2 in a boy with developmental delay, deficits in speech and language without autistic behaviorsHaiming Yuan, Xiaoxiu Li, Qingming Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 27, 2020
[Identification of a de novo MAP2K1 gene variant in an affected patient with Cardio-facio-cutaneous syndrome]Qingming Wang, Pengliang Chen, Qian Peng, et al.
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