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Chunyu Luo

Showing results (11-20 of 63) with videos related to

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Molecular Medicine Reports|January 20, 2016
Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysisDingyuan Ma, Jingjing Zhang, Chunyu Luo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2022
[Prenatal diagnosis of fetuses with renal anomalies by whole genome sequencing]Fengchang Qiao, Ping Hu, Cuiping Zhang, et al.
Toxicology Research|June 30, 2025
Network toxicology and immune-metabolic dysregulation: linking per- and polyfluoroalkyl substances exposure to osteoarthritis pathogenesisQian Zhang, Wenqi Zhang, Zhuchen Liu, et al.
Journal of Environmental Management|January 4, 2019
Identifying restoration priorities for wetlands based on historical distributions of biodiversity features and restoration suitabilityYi Qu, Gongqi Sun, Chunyu Luo, et al.
Journal of Clinical Laboratory Analysis|November 28, 2022
Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiencyJingjing Zhang, Dingyuan Ma, Gang Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2014
[Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis]Jingjing Zhang, Ping Hu, Chunyu Luo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 2024
A case of transient elevation of creatinine caused by severe hyperuricemiaQiong Wu, Yumeng Gao, Xinyuan Zhang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 6, 2023
Next-generation sequencing for genetic testing of hearing loss populationsLulu Wang, Gang Liu, Dingyuan Ma, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencingFengchang Qiao, Chen Wang, Chunyu Luo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Detection of TSC1/TSC2 gene mutations among patients with tuberous sclerosis complex by Ion Torrent semiconductor sequencing]Yuguo Wang, Ying Lin, Chunyu Luo, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

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Pageof 7
Molecular Medicine Reports|January 20, 2016
Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysisDingyuan Ma, Jingjing Zhang, Chunyu Luo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2022
[Prenatal diagnosis of fetuses with renal anomalies by whole genome sequencing]Fengchang Qiao, Ping Hu, Cuiping Zhang, et al.
Toxicology Research|June 30, 2025
Network toxicology and immune-metabolic dysregulation: linking per- and polyfluoroalkyl substances exposure to osteoarthritis pathogenesisQian Zhang, Wenqi Zhang, Zhuchen Liu, et al.
Journal of Environmental Management|January 4, 2019
Identifying restoration priorities for wetlands based on historical distributions of biodiversity features and restoration suitabilityYi Qu, Gongqi Sun, Chunyu Luo, et al.
Journal of Clinical Laboratory Analysis|November 28, 2022
Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiencyJingjing Zhang, Dingyuan Ma, Gang Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2014
[Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis]Jingjing Zhang, Ping Hu, Chunyu Luo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 2024
A case of transient elevation of creatinine caused by severe hyperuricemiaQiong Wu, Yumeng Gao, Xinyuan Zhang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 6, 2023
Next-generation sequencing for genetic testing of hearing loss populationsLulu Wang, Gang Liu, Dingyuan Ma, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencingFengchang Qiao, Chen Wang, Chunyu Luo, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Detection of TSC1/TSC2 gene mutations among patients with tuberous sclerosis complex by Ion Torrent semiconductor sequencing]Yuguo Wang, Ying Lin, Chunyu Luo, et al.
Pageof 7