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Chunyu Luo

Showing results (31-40 of 63) with videos related to

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The Science of the Total Environment|November 25, 2021
Estimation of wetland biodiversity based on the hydrological patterns and connectivity and its potential application in change detection and monitoring: A case study of the Sanjiang Plain, ChinaYi Qu, Yaomin Zheng, Peng Gong, et al.
Clinical Chemistry and Laboratory Medicine|November 19, 2024
Expanded carrier screening for 224 monogenic disease genes in 1,499 Chinese couples: a single-center studyJianxin Tan, Juan Tan, Zhu Jiang, et al.
Frontiers in Genetics|March 1, 2018
Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular DystrophyJing Zhou, Jianxin Tan, Dingyuan Ma, et al.
Molecular Genetics & Genomic Medicine|March 24, 2026
Clinical Utility of Prenatal cfDNA Screening for Sex Chromosome Aneuploidies: A Single Center ExperienceYing Lin, Qun Lu, Yun Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 5, 2018
[Genetic analysis and prenatal diagnosis for 25 Chinese pedigrees affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]Chunyu Luo, Tao Jiang, Jingjing Zhang, et al.
The Journal of Molecular Diagnostics : JMD|March 25, 2020
Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy in 13,069 Chinese Pregnant WomenJingjing Zhang, Yuguo Wang, Dingyuan Ma, et al.
Frontiers in Genetics|May 10, 2018
A Novel Whole Gene Deletion of <i>BCKDHB</i> by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine DiseaseGang Liu, Dingyuan Ma, Ping Hu, et al.
BMC Medical Genetics|April 14, 2018
Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case reportGang Liu, Dingyuan Ma, Jian Cheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2017
[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome]Xiuqing Ji, Huanran Hu, Yan Wang, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|April 19, 2024
Increased SERPINB2 potentiates 15LO1 expression via STAT6 signalling in epithelial cells in eosinophilic chronic rhinosinusitis with nasal polypsChunyu Luo, Ying Zhu, Shiyao Zhang, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
The Science of the Total Environment|November 25, 2021
Estimation of wetland biodiversity based on the hydrological patterns and connectivity and its potential application in change detection and monitoring: A case study of the Sanjiang Plain, ChinaYi Qu, Yaomin Zheng, Peng Gong, et al.
Clinical Chemistry and Laboratory Medicine|November 19, 2024
Expanded carrier screening for 224 monogenic disease genes in 1,499 Chinese couples: a single-center studyJianxin Tan, Juan Tan, Zhu Jiang, et al.
Frontiers in Genetics|March 1, 2018
Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular DystrophyJing Zhou, Jianxin Tan, Dingyuan Ma, et al.
Molecular Genetics & Genomic Medicine|March 24, 2026
Clinical Utility of Prenatal cfDNA Screening for Sex Chromosome Aneuploidies: A Single Center ExperienceYing Lin, Qun Lu, Yun Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 5, 2018
[Genetic analysis and prenatal diagnosis for 25 Chinese pedigrees affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]Chunyu Luo, Tao Jiang, Jingjing Zhang, et al.
The Journal of Molecular Diagnostics : JMD|March 25, 2020
Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy in 13,069 Chinese Pregnant WomenJingjing Zhang, Yuguo Wang, Dingyuan Ma, et al.
Frontiers in Genetics|May 10, 2018
A Novel Whole Gene Deletion of <i>BCKDHB</i> by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine DiseaseGang Liu, Dingyuan Ma, Ping Hu, et al.
BMC Medical Genetics|April 14, 2018
Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case reportGang Liu, Dingyuan Ma, Jian Cheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2017
[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome]Xiuqing Ji, Huanran Hu, Yan Wang, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|April 19, 2024
Increased SERPINB2 potentiates 15LO1 expression via STAT6 signalling in epithelial cells in eosinophilic chronic rhinosinusitis with nasal polypsChunyu Luo, Ying Zhu, Shiyao Zhang, et al.
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