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Shaobin Lin

Showing results (61-70 of 92) with videos related to

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BMC Medical Genetics|April 18, 2018
A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature reviewYanwei Sha, Liangkai Zheng, Zhiyong Ji, et al.
Frontiers in Genetics|March 22, 2021
Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese FamilyShaobin Lin, Zhiming He, Linhuan Huang, et al.
Molecular Cytogenetics|January 4, 2024
Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort studyShaobin Lin, Shanshan Shi, Jian Lu, et al.
Prenatal Diagnosis|February 21, 2018
Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twinsYi Zhang, Linhuan Huang, Xuan Huang, et al.
Thrombosis and Haemostasis|March 17, 2025
Clinical Phenotype and Genetic Analysis of a Family with Hereditary Antithrombin Deficiency Caused by SERPINC1 Gene MutationYating Zhao, Longting Du, Shaobin Lin, et al.
Electrophoresis|April 7, 2020
Noninvasive prenatal paternity testing by maternal plasma DNA sequencing in twin pregnanciesYifan Xie, Ning Qu, Shaobin Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 15, 2015
[Chromosomal microarray analysis for lateral ventriculomegaly in fetus]Zhiqiang Zhang, Yingjun Xie, Jianzhu Wu, et al.
Talanta|October 15, 2024
Simple and rapid multicolor sensor for seminal plasma ROS detection based on synergistic catalytic etching of gold nanobipyramids dopped agarose composite gelYating Liu, Lingjun Cheng, Shaobin Lin, et al.
Transfusion|March 15, 2018
Noninvasive prenatal paternity testing using targeted massively parallel sequencingNing- Qu, Yifan Xie, Haiyan Li, et al.
Journal of Human Genetics|June 20, 2020
Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotypeYanwei Sha, Xiaoli Wei, Lu Ding, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
BMC Medical Genetics|April 18, 2018
A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature reviewYanwei Sha, Liangkai Zheng, Zhiyong Ji, et al.
Frontiers in Genetics|March 22, 2021
Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese FamilyShaobin Lin, Zhiming He, Linhuan Huang, et al.
Molecular Cytogenetics|January 4, 2024
Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort studyShaobin Lin, Shanshan Shi, Jian Lu, et al.
Prenatal Diagnosis|February 21, 2018
Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twinsYi Zhang, Linhuan Huang, Xuan Huang, et al.
Thrombosis and Haemostasis|March 17, 2025
Clinical Phenotype and Genetic Analysis of a Family with Hereditary Antithrombin Deficiency Caused by SERPINC1 Gene MutationYating Zhao, Longting Du, Shaobin Lin, et al.
Electrophoresis|April 7, 2020
Noninvasive prenatal paternity testing by maternal plasma DNA sequencing in twin pregnanciesYifan Xie, Ning Qu, Shaobin Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 15, 2015
[Chromosomal microarray analysis for lateral ventriculomegaly in fetus]Zhiqiang Zhang, Yingjun Xie, Jianzhu Wu, et al.
Talanta|October 15, 2024
Simple and rapid multicolor sensor for seminal plasma ROS detection based on synergistic catalytic etching of gold nanobipyramids dopped agarose composite gelYating Liu, Lingjun Cheng, Shaobin Lin, et al.
Transfusion|March 15, 2018
Noninvasive prenatal paternity testing using targeted massively parallel sequencingNing- Qu, Yifan Xie, Haiyan Li, et al.
Journal of Human Genetics|June 20, 2020
Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotypeYanwei Sha, Xiaoli Wei, Lu Ding, et al.
Pageof 10