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Jiasun Su

Showing results (1-10 of 42) with videos related to

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The Journal of Obstetrics and Gynaecology Research|September 27, 2021
Study on the correlation between the ultrasound phenotype and copy number variation of abnormal embryo in spontaneous abortionShuyin Tan, Pingshan Pan, Zuojian Yang, et al.
International Journal of General Medicine|August 14, 2023
Genetic Basis of Congenital Central Hypothyroidism in Children: Expanding the Mutational Spectrum of POU1F1 and ATP6V0A4Chunyun Fu, Jingsi Luo, Jiasun Su, et al.
Experimental and Therapeutic Medicine|May 26, 2021
Clinical application of whole-exome sequencing: A retrospective, single-center studyQiang Zhang, Zailong Qin, Shang Yi, et al.
BMC Medical Genomics|December 11, 2020
Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literatureQiang Zhang, Zailong Qin, Shang Yi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2022
[Comparison of performance of two prenatal diagnostic techniques for the detection of chromosomal mosaicisms in amniocytes]Weijia Sun, Jiasun Su, Tiansheng Liu, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 11, 2024
Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control studyLinlin Wang, Ping Liang, Pingshan Pan, et al.
Translational Pediatrics|June 15, 2026
Rare 19q13.42 duplication encompassing <i>PRKCG</i> associated with neurodevelopmental abnormalitiesJiasun Su, Lin Yang, Huiping Li, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 3, 2021
The application of expanded noninvasive prenatal screening for genome-wide chromosomal abnormalities and genetic counselingYun Chen, Yunli Lai, Fuben Xu, et al.
Journal of Pregnancy|November 21, 2025
Analysis of Prenatal Diagnosis and Pregnancy Decisions of 767 Singleton Pregnancies With Positive Prenatal Cell-Free DNA Screening Results in Southwest ChinaYun Chen, Yunli Lai, Fuben Xu, et al.
BMC Medical Genetics|May 13, 2020
A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5Wei Li, Xin Fan, Yue Zhang, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
The Journal of Obstetrics and Gynaecology Research|September 27, 2021
Study on the correlation between the ultrasound phenotype and copy number variation of abnormal embryo in spontaneous abortionShuyin Tan, Pingshan Pan, Zuojian Yang, et al.
International Journal of General Medicine|August 14, 2023
Genetic Basis of Congenital Central Hypothyroidism in Children: Expanding the Mutational Spectrum of POU1F1 and ATP6V0A4Chunyun Fu, Jingsi Luo, Jiasun Su, et al.
Experimental and Therapeutic Medicine|May 26, 2021
Clinical application of whole-exome sequencing: A retrospective, single-center studyQiang Zhang, Zailong Qin, Shang Yi, et al.
BMC Medical Genomics|December 11, 2020
Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literatureQiang Zhang, Zailong Qin, Shang Yi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2022
[Comparison of performance of two prenatal diagnostic techniques for the detection of chromosomal mosaicisms in amniocytes]Weijia Sun, Jiasun Su, Tiansheng Liu, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 11, 2024
Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control studyLinlin Wang, Ping Liang, Pingshan Pan, et al.
Translational Pediatrics|June 15, 2026
Rare 19q13.42 duplication encompassing <i>PRKCG</i> associated with neurodevelopmental abnormalitiesJiasun Su, Lin Yang, Huiping Li, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 3, 2021
The application of expanded noninvasive prenatal screening for genome-wide chromosomal abnormalities and genetic counselingYun Chen, Yunli Lai, Fuben Xu, et al.
Journal of Pregnancy|November 21, 2025
Analysis of Prenatal Diagnosis and Pregnancy Decisions of 767 Singleton Pregnancies With Positive Prenatal Cell-Free DNA Screening Results in Southwest ChinaYun Chen, Yunli Lai, Fuben Xu, et al.
BMC Medical Genetics|May 13, 2020
A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5Wei Li, Xin Fan, Yue Zhang, et al.
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