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Yuanbai Wang

Showing results (11-20 of 28) with videos related to

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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 29, 2021
[The value of combined detection of HbA2 and HbF for the screening of thalassemia among individuals of childbearing ages]Qianmei Zhuang, Geng Wang, Yuanbai Wang, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|January 26, 2023
A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign VariantJianlong Zhuang, Qi Luo, Shuhong Zeng, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the <i>KCNH2</i> Gene in a Fetus With Familial 2q14.2 DuplicationJianlong Zhuang, Chunnuan Chen, Yuanbai Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2022
[Genetic analysis of a case with a supernumerary marker derived from chromosome 9]Qianmei Zhuang, Meizhen Yan, Yuying Jiang, et al.
Frontiers in Genetics|October 18, 2021
Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective StudyJianlong Zhuang, Na Zhang, Yuanbai Wang, et al.
Journal of Clinical Pathology|February 29, 2020
Identification of a new β-thalassaemia variant Term CD+32(HBB: c.32A>C) in two Chinese familiesJianlong Zhuang, Yu Zheng, Yuanbai Wang, et al.
Molecular Cytogenetics|June 7, 2022
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese populationJianlong Zhuang, Chunnuan Chen, Rongfu Huang, et al.
BMC Pregnancy and Childbirth|January 29, 2021
Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, ChinaJianlong Zhuang, Chunnuan Chen, Yuying Jiang, et al.
Molecular Cytogenetics|September 30, 2021
Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism arrayJianlong Zhuang, Na Zhang, Wanyu Fu, et al.
Molecular Genetics & Genomic Medicine|December 12, 2022
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature reviewJianlong Zhuang, Qi Luo, Meihua Xie, et al.
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Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 29, 2021
[The value of combined detection of HbA2 and HbF for the screening of thalassemia among individuals of childbearing ages]Qianmei Zhuang, Geng Wang, Yuanbai Wang, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|January 26, 2023
A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign VariantJianlong Zhuang, Qi Luo, Shuhong Zeng, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the <i>KCNH2</i> Gene in a Fetus With Familial 2q14.2 DuplicationJianlong Zhuang, Chunnuan Chen, Yuanbai Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2022
[Genetic analysis of a case with a supernumerary marker derived from chromosome 9]Qianmei Zhuang, Meizhen Yan, Yuying Jiang, et al.
Frontiers in Genetics|October 18, 2021
Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective StudyJianlong Zhuang, Na Zhang, Yuanbai Wang, et al.
Journal of Clinical Pathology|February 29, 2020
Identification of a new β-thalassaemia variant Term CD+32(HBB: c.32A>C) in two Chinese familiesJianlong Zhuang, Yu Zheng, Yuanbai Wang, et al.
Molecular Cytogenetics|June 7, 2022
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese populationJianlong Zhuang, Chunnuan Chen, Rongfu Huang, et al.
BMC Pregnancy and Childbirth|January 29, 2021
Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, ChinaJianlong Zhuang, Chunnuan Chen, Yuying Jiang, et al.
Molecular Cytogenetics|September 30, 2021
Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism arrayJianlong Zhuang, Na Zhang, Wanyu Fu, et al.
Molecular Genetics & Genomic Medicine|December 12, 2022
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature reviewJianlong Zhuang, Qi Luo, Meihua Xie, et al.
Pageof 3