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Yanjie Fan

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

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Molecular Cytogenetics|February 18, 2016
Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarrayGuorui Hu, Yanjie Fan, Lili Wang, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|July 11, 2018
A Functional Mutation in HDAC8 Gene as Novel Diagnostic Marker for Cornelia De Lange SyndromeXueren Gao, Zhuo Huang, Yanjie Fan, et al.
Journal of Molecular Neuroscience : MN|January 6, 2021
Chronic Neuroinflammation Induced by Lipopolysaccharide Injection into the Third Ventricle Induces Behavioral ChangesShufang Na, Xuejiao Duan, Rongyan Wang, et al.
American Journal of Medical Genetics. Part A|October 21, 2016
Further delineation of the phenotype of truncating KMT2A mutations: The extended Wiedemann-Steiner syndromeYu Sun, Guorui Hu, Huili Liu, et al.
Clinical Genetics|October 30, 2022
Improving variant prioritization in exome analysis by entropy-weighted ensemble of multiple toolsYanjie Fan, Ying Zhou, Huili Liu, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 12, 2019
A Novel Nonsense Mutation of <i>PHF6</i> in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann SyndromeXia Zhang, Yanjie Fan, Xiaomin Liu, et al.
Clinical Chemistry and Laboratory Medicine|July 18, 2024
Clinical utility of regions of homozygosity (ROH) identified in exome sequencing: when to pursue confirmatory uniparental disomy testing for imprinting disorders?Xiaoyan Huo, Xinyi Lu, Deyun Lu, et al.
Plant Physiology|January 8, 2026
CitNOR-like1 is conserved in the regulation of ascorbic acid accumulation in plantsZiang Liu, Guanglian Liao, Yanjie Fan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 14, 2018
[Clinical phenotypes and genetic study of 2 cases with 22q13 deletion syndrome]Jihang Luo, Di Fang, Wenjuan Qiu, et al.
World Journal of Urology|September 16, 2020
Integration of exome sequencing and metabolic evaluation for the diagnosis of children with urolithiasisYining Zhao, Xiaoliang Fang, Yanjie Fan, et al.
Pageof 6

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

Sort By:
Pageof 6
Molecular Cytogenetics|February 18, 2016
Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarrayGuorui Hu, Yanjie Fan, Lili Wang, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|July 11, 2018
A Functional Mutation in HDAC8 Gene as Novel Diagnostic Marker for Cornelia De Lange SyndromeXueren Gao, Zhuo Huang, Yanjie Fan, et al.
Journal of Molecular Neuroscience : MN|January 6, 2021
Chronic Neuroinflammation Induced by Lipopolysaccharide Injection into the Third Ventricle Induces Behavioral ChangesShufang Na, Xuejiao Duan, Rongyan Wang, et al.
American Journal of Medical Genetics. Part A|October 21, 2016
Further delineation of the phenotype of truncating KMT2A mutations: The extended Wiedemann-Steiner syndromeYu Sun, Guorui Hu, Huili Liu, et al.
Clinical Genetics|October 30, 2022
Improving variant prioritization in exome analysis by entropy-weighted ensemble of multiple toolsYanjie Fan, Ying Zhou, Huili Liu, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 12, 2019
A Novel Nonsense Mutation of <i>PHF6</i> in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann SyndromeXia Zhang, Yanjie Fan, Xiaomin Liu, et al.
Clinical Chemistry and Laboratory Medicine|July 18, 2024
Clinical utility of regions of homozygosity (ROH) identified in exome sequencing: when to pursue confirmatory uniparental disomy testing for imprinting disorders?Xiaoyan Huo, Xinyi Lu, Deyun Lu, et al.
Plant Physiology|January 8, 2026
CitNOR-like1 is conserved in the regulation of ascorbic acid accumulation in plantsZiang Liu, Guanglian Liao, Yanjie Fan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 14, 2018
[Clinical phenotypes and genetic study of 2 cases with 22q13 deletion syndrome]Jihang Luo, Di Fang, Wenjuan Qiu, et al.
World Journal of Urology|September 16, 2020
Integration of exome sequencing and metabolic evaluation for the diagnosis of children with urolithiasisYining Zhao, Xiaoliang Fang, Yanjie Fan, et al.
Pageof 6