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Chunnuan Chen

Showing results (11-20 of 64) with videos related to

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Molecular Cytogenetics|August 2, 2023
Identification of a novel isolated 4q35.2 microdeletion in a Chinese pediatric patient using chromosomal microarray analysis: a case report and literature reviewJianlong Zhuang, Shufen Liu, Xinying Chen, et al.
BMC Pregnancy and Childbirth|April 26, 2026
Prenatal diagnosis and molecular cytogenetic analysis of Xp22.31 microdeletions and microduplications in Chinese populationsJianlong Zhuang, Wanyu Fu, Yu'e Chen, et al.
Annals of Hematology|April 9, 2026
First clinical and molecular characterization of two rare complex β-globin variants in Chinese population using third generation sequencingLixian Zhang, Jianlong Zhuang, Nan Huang, et al.
Translational Psychiatry|October 6, 2019
Identification of HIVEP2 as a dopaminergic transcription factor related to substance use disorders in rats and humansJuan Zhao, Chunnuan Chen, Richard L Bell, et al.
BMC Pregnancy and Childbirth|July 19, 2025
Prenatal diagnosis and genetic assessment of fetuses with single umbilical artery using chromosomal microarray analysis: a seven-year single-center retrospective studyJianlong Zhuang, Nan Huang, Yu'e Chen, et al.
Brain Tumor Pathology|February 16, 2026
Rare intracranial mesenchymal tumors with FET::CREB fusions: clinicopathologic spectrum of four cases with integrated molecular analysis and review of the literatureXiaoqun Ba, Wanli Huang, Shufen Liu, et al.
Molecular Genetics & Genomic Medicine|March 30, 2024
Initial clinical and molecular investigation of 20q13.33 microdeletion with 17q25.3/14q32.31q32.33 microduplication in Chinese pediatric patientsJianlong Zhuang, Na Zhang, Junyu Wang, et al.
European Journal of Medical Research|July 2, 2025
Etiological diagnosis of miscarriage by combining use of chromosomal microarray analysis and whole-exome sequencingJianlong Zhuang, Wanyu Fu, Ling Gu, et al.
Molecular Cytogenetics|September 1, 2024
Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective studyJianlong Zhuang, Na Zhang, Wanyu Fu, et al.
Molecular Genetics & Genomic Medicine|January 29, 2024
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese populationJianlong Zhuang, Yuying Jiang, Yu'e Chen, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Molecular Cytogenetics|August 2, 2023
Identification of a novel isolated 4q35.2 microdeletion in a Chinese pediatric patient using chromosomal microarray analysis: a case report and literature reviewJianlong Zhuang, Shufen Liu, Xinying Chen, et al.
BMC Pregnancy and Childbirth|April 26, 2026
Prenatal diagnosis and molecular cytogenetic analysis of Xp22.31 microdeletions and microduplications in Chinese populationsJianlong Zhuang, Wanyu Fu, Yu'e Chen, et al.
Annals of Hematology|April 9, 2026
First clinical and molecular characterization of two rare complex β-globin variants in Chinese population using third generation sequencingLixian Zhang, Jianlong Zhuang, Nan Huang, et al.
Translational Psychiatry|October 6, 2019
Identification of HIVEP2 as a dopaminergic transcription factor related to substance use disorders in rats and humansJuan Zhao, Chunnuan Chen, Richard L Bell, et al.
BMC Pregnancy and Childbirth|July 19, 2025
Prenatal diagnosis and genetic assessment of fetuses with single umbilical artery using chromosomal microarray analysis: a seven-year single-center retrospective studyJianlong Zhuang, Nan Huang, Yu'e Chen, et al.
Brain Tumor Pathology|February 16, 2026
Rare intracranial mesenchymal tumors with FET::CREB fusions: clinicopathologic spectrum of four cases with integrated molecular analysis and review of the literatureXiaoqun Ba, Wanli Huang, Shufen Liu, et al.
Molecular Genetics & Genomic Medicine|March 30, 2024
Initial clinical and molecular investigation of 20q13.33 microdeletion with 17q25.3/14q32.31q32.33 microduplication in Chinese pediatric patientsJianlong Zhuang, Na Zhang, Junyu Wang, et al.
European Journal of Medical Research|July 2, 2025
Etiological diagnosis of miscarriage by combining use of chromosomal microarray analysis and whole-exome sequencingJianlong Zhuang, Wanyu Fu, Ling Gu, et al.
Molecular Cytogenetics|September 1, 2024
Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective studyJianlong Zhuang, Na Zhang, Wanyu Fu, et al.
Molecular Genetics & Genomic Medicine|January 29, 2024
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese populationJianlong Zhuang, Yuying Jiang, Yu'e Chen, et al.
Pageof 7