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Zirui Dong

Showing results (51-60 of 66) with videos related to

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Prenatal Diagnosis|February 18, 2026
NONO-Related Syndromic X-Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal CohortYilin Zhao, Gang Zou, Mengmeng Shi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approachZirui Dong, Jun Zhang, Ping Hu, et al.
Genome Biology|January 31, 2015
An investigation of biomarkers derived from legacy microarray data for their utility in the RNA-seq eraZhenqiang Su, Hong Fang, Huixiao Hong, et al.
Frontiers in Genetics|September 3, 2019
Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing AnalysisKwong Wai Choy, Huilin Wang, Mengmeng Shi, et al.
Diagnostics (Basel, Switzerland)|June 12, 2026
Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype-Phenotype Correlations, and OutcomesYu Zheng, Mengmeng Shi, Yilin Zhao, et al.
Human Mutation|March 11, 2014
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencingZirui Dong, Lupin Jiang, Chuanchun Yang, et al.
Human Genetics|May 27, 2020
Low-pass genome sequencing: a validated method in clinical cytogeneticsMatthew Hoi Kin Chau, Huilin Wang, Yunli Lai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2017
Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogeneticsZirui Dong, Huilin Wang, Haixiao Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 27, 2019
Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosisHuilin Wang, Zirui Dong, Rui Zhang, et al.
The Journal of Investigative Dermatology|May 13, 2019
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human DiseasesQi Zhen, Zhenjun Yang, Wenjun Wang, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|February 18, 2026
NONO-Related Syndromic X-Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal CohortYilin Zhao, Gang Zou, Mengmeng Shi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approachZirui Dong, Jun Zhang, Ping Hu, et al.
Genome Biology|January 31, 2015
An investigation of biomarkers derived from legacy microarray data for their utility in the RNA-seq eraZhenqiang Su, Hong Fang, Huixiao Hong, et al.
Frontiers in Genetics|September 3, 2019
Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing AnalysisKwong Wai Choy, Huilin Wang, Mengmeng Shi, et al.
Diagnostics (Basel, Switzerland)|June 12, 2026
Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype-Phenotype Correlations, and OutcomesYu Zheng, Mengmeng Shi, Yilin Zhao, et al.
Human Mutation|March 11, 2014
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencingZirui Dong, Lupin Jiang, Chuanchun Yang, et al.
Human Genetics|May 27, 2020
Low-pass genome sequencing: a validated method in clinical cytogeneticsMatthew Hoi Kin Chau, Huilin Wang, Yunli Lai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2017
Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogeneticsZirui Dong, Huilin Wang, Haixiao Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 27, 2019
Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosisHuilin Wang, Zirui Dong, Rui Zhang, et al.
The Journal of Investigative Dermatology|May 13, 2019
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human DiseasesQi Zhen, Zhenjun Yang, Wenjun Wang, et al.
Pageof 7