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Jiale Xiang

Showing results (21-30 of 32) with videos related to

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Scientific Reports|July 9, 2025
Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndromeJiale Xiang, Xiangzhong Sun, Jiguang Peng, et al.
Human Genetics|February 1, 2020
Concurrent hearing and genetic screening in a general newborn populationLing Guo, Jiale Xiang, Lei Sun, et al.
Human Genomics|February 14, 2026
Concurrent physiologic and gene-based genetic newborn hearing screening in a general populationYun Sun, Jingyu Zhao, Liping Meng, et al.
Oncology Letters|March 15, 2019
Novel loss-of-function mutation in <i>BRCA2</i> gene identified in a Chinese female with a family history of ovarian cancer: A case reportYanzhi Cui, Yanyan Wang, Ningzhi Zhang, et al.
BMC Genomics|October 7, 2021
AutoCNV: a semiautomatic CNV interpretation system based on the 2019 ACMG/ClinGen Technical Standards for CNVsChunna Fan, Zhonghua Wang, Yan Sun, et al.
BMC Genomics|February 10, 2026
Generation of quartet reference materials for preimplantation genetic testing for structural rearrangementsNan Sun, Wenxin Zhang, Dandan Yu, et al.
BMC Medical Genomics|November 9, 2019
Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysisHaining Luo, Chao Chen, Yun Yang, et al.
Nature Plants|October 10, 2019
Transcriptional regulatory framework for vascular cambium development in Arabidopsis rootsJing Zhang, Gugan Eswaran, Juan Alonso-Serra, et al.
American Journal of Obstetrics & Gynecology MFM|November 15, 2022
Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomyJiale Xiang, Ru Li, Jun He, et al.
JAMA Network Open|September 1, 2023
Genomic Sequencing as a First-Tier Screening Test and Outcomes of Newborn ScreeningTing Chen, Chunna Fan, Yonglan Huang, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Scientific Reports|July 9, 2025
Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndromeJiale Xiang, Xiangzhong Sun, Jiguang Peng, et al.
Human Genetics|February 1, 2020
Concurrent hearing and genetic screening in a general newborn populationLing Guo, Jiale Xiang, Lei Sun, et al.
Human Genomics|February 14, 2026
Concurrent physiologic and gene-based genetic newborn hearing screening in a general populationYun Sun, Jingyu Zhao, Liping Meng, et al.
Oncology Letters|March 15, 2019
Novel loss-of-function mutation in <i>BRCA2</i> gene identified in a Chinese female with a family history of ovarian cancer: A case reportYanzhi Cui, Yanyan Wang, Ningzhi Zhang, et al.
BMC Genomics|October 7, 2021
AutoCNV: a semiautomatic CNV interpretation system based on the 2019 ACMG/ClinGen Technical Standards for CNVsChunna Fan, Zhonghua Wang, Yan Sun, et al.
BMC Genomics|February 10, 2026
Generation of quartet reference materials for preimplantation genetic testing for structural rearrangementsNan Sun, Wenxin Zhang, Dandan Yu, et al.
BMC Medical Genomics|November 9, 2019
Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysisHaining Luo, Chao Chen, Yun Yang, et al.
Nature Plants|October 10, 2019
Transcriptional regulatory framework for vascular cambium development in Arabidopsis rootsJing Zhang, Gugan Eswaran, Juan Alonso-Serra, et al.
American Journal of Obstetrics & Gynecology MFM|November 15, 2022
Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomyJiale Xiang, Ru Li, Jun He, et al.
JAMA Network Open|September 1, 2023
Genomic Sequencing as a First-Tier Screening Test and Outcomes of Newborn ScreeningTing Chen, Chunna Fan, Yonglan Huang, et al.
Pageof 4