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Yeqing Qian

Showing results (41-50 of 57) with videos related to

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Frontiers in Immunology|December 27, 2021
Pro-Inflammatory Signature in Decidua of Recurrent Pregnancy Loss Regardless of Embryonic Chromosomal AbnormalitiesZaigui Wu, Miaomiao Wang, Guanmian Liang, et al.
The Journal of Gene Medicine|March 26, 2022
Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 genePeng Wang, Pengzhen Jin, Linyan Zhu, et al.
Expert Review of Molecular Diagnostics|March 25, 2024
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnanciesYanfei Xu, Jianbo Lou, Yeqing Qian, et al.
Molecular Therapy. Nucleic Acids|December 23, 2021
circRNA-DURSA regulates trophoblast apoptosis via miR-760-HIST1H2BE axis in unexplained recurrent spontaneous abortionMinyue Tang, Long Bai, Zhe Wan, et al.
Orphanet Journal of Rare Diseases|June 13, 2026
Diagnosis of de novo fetal aceruloplasminemia via whole exome sequencing and fetal umbilical blood ceruloplasmin measurementPengzhen Jin, Guangmei Dai, Jiawei Hong, et al.
Frontiers in Genetics|December 17, 2020
Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1Songchang Chen, Weihui Shi, Yeqing Qian, et al.
BMC Medical Genomics|June 27, 2024
Identification of four TTN variants in three families with fetal akinesia deformation sequenceLihong Fan, Haibo Li, Ying Xu, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 4, 2023
Noninvasive Prenatal Screening for Common Fetal Aneuploidies Using Single-Molecule SequencingYeqing Qian, Yongfeng Liu, Kai Yan, et al.
BMC Medical Genomics|November 22, 2025
Performance testing for the sensitivity and resolution of low-pass WGS for small CNV detectionShuhui Huang, Juan Li, Danping Liu, et al.
Prenatal Diagnosis|December 16, 2016
A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimensSongchang Chen, Deyuan Liu, Junyu Zhang, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Frontiers in Immunology|December 27, 2021
Pro-Inflammatory Signature in Decidua of Recurrent Pregnancy Loss Regardless of Embryonic Chromosomal AbnormalitiesZaigui Wu, Miaomiao Wang, Guanmian Liang, et al.
The Journal of Gene Medicine|March 26, 2022
Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 genePeng Wang, Pengzhen Jin, Linyan Zhu, et al.
Expert Review of Molecular Diagnostics|March 25, 2024
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnanciesYanfei Xu, Jianbo Lou, Yeqing Qian, et al.
Molecular Therapy. Nucleic Acids|December 23, 2021
circRNA-DURSA regulates trophoblast apoptosis via miR-760-HIST1H2BE axis in unexplained recurrent spontaneous abortionMinyue Tang, Long Bai, Zhe Wan, et al.
Orphanet Journal of Rare Diseases|June 13, 2026
Diagnosis of de novo fetal aceruloplasminemia via whole exome sequencing and fetal umbilical blood ceruloplasmin measurementPengzhen Jin, Guangmei Dai, Jiawei Hong, et al.
Frontiers in Genetics|December 17, 2020
Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1Songchang Chen, Weihui Shi, Yeqing Qian, et al.
BMC Medical Genomics|June 27, 2024
Identification of four TTN variants in three families with fetal akinesia deformation sequenceLihong Fan, Haibo Li, Ying Xu, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 4, 2023
Noninvasive Prenatal Screening for Common Fetal Aneuploidies Using Single-Molecule SequencingYeqing Qian, Yongfeng Liu, Kai Yan, et al.
BMC Medical Genomics|November 22, 2025
Performance testing for the sensitivity and resolution of low-pass WGS for small CNV detectionShuhui Huang, Juan Li, Danping Liu, et al.
Prenatal Diagnosis|December 16, 2016
A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimensSongchang Chen, Deyuan Liu, Junyu Zhang, et al.
Pageof 6