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Meihuan Chen

Showing results (31-40 of 54) with videos related to

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International Journal of Clinical and Experimental Pathology|January 15, 2020
Identification of a novel pre-terminating mutation in human HBB gene as a cause of β<sup>0</sup>-thalassemia phenotypeLiangpu Xu, Meihuan Chen, Hailong Huang, et al.
International Journal of Clinical and Experimental Pathology|January 18, 2020
A rare α-thalassemia deletion, -α<sup>27.6</sup>, is identified from three Chinese families in Fujian provinceHailong Huang, Meihuan Chen, Xuemei Chen, et al.
Genetics Research|June 17, 2025
Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern ChinaJunhao Zheng, Meihuan Chen, Siwen Zhang, et al.
Molecular Reproduction and Development|December 17, 2017
Application of the BACs-on-Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletionsHailong Huang, Min Zhang, Yan Wang, et al.
BMC Pregnancy and Childbirth|October 11, 2025
Detection of chromosomal and gene abnormality with karyotyping, chromosomal microarray analysis and trio-based whole exome sequencing in pregnancies with fetal growth restriction: implications for precise prenatal diagnosisYangping Chen, Meiying Cai, Meihuan Chen, et al.
Plos One|October 5, 2023
The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expressionMeihuan Chen, Xinrui Wang, Haiwei Wang, 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|September 6, 2023
Identification of a novel 91.5 kb-deletion (αα)<sup>FJ</sup> in the α-globin gene cluster using single-molecule real-time (SMRT) sequencingLiangpu Xu, Meihuan Chen, Junhao Zheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2017
[Prenatal diagnosis of a fetus with Miller-Dieker syndrome]Liangpu Xu, Hailong Huang, Yan Wang, et al.
Journal of Clinical Laboratory Analysis|January 17, 2020
X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestationsMin Zhang, Hailong Huang, Na Lin, et al.
Cellular and Molecular Life Sciences : CMLS|March 6, 2026
Circ_0001428 regulates erythropoiesis and γ-globin expression via activating the ATF4-BCL11A axis in β-thalassemiaJingmin Li, Yali Pan, Meihuan Chen, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
International Journal of Clinical and Experimental Pathology|January 15, 2020
Identification of a novel pre-terminating mutation in human HBB gene as a cause of β<sup>0</sup>-thalassemia phenotypeLiangpu Xu, Meihuan Chen, Hailong Huang, et al.
International Journal of Clinical and Experimental Pathology|January 18, 2020
A rare α-thalassemia deletion, -α<sup>27.6</sup>, is identified from three Chinese families in Fujian provinceHailong Huang, Meihuan Chen, Xuemei Chen, et al.
Genetics Research|June 17, 2025
Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern ChinaJunhao Zheng, Meihuan Chen, Siwen Zhang, et al.
Molecular Reproduction and Development|December 17, 2017
Application of the BACs-on-Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletionsHailong Huang, Min Zhang, Yan Wang, et al.
BMC Pregnancy and Childbirth|October 11, 2025
Detection of chromosomal and gene abnormality with karyotyping, chromosomal microarray analysis and trio-based whole exome sequencing in pregnancies with fetal growth restriction: implications for precise prenatal diagnosisYangping Chen, Meiying Cai, Meihuan Chen, et al.
Plos One|October 5, 2023
The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expressionMeihuan Chen, Xinrui Wang, Haiwei Wang, 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|September 6, 2023
Identification of a novel 91.5 kb-deletion (αα)<sup>FJ</sup> in the α-globin gene cluster using single-molecule real-time (SMRT) sequencingLiangpu Xu, Meihuan Chen, Junhao Zheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2017
[Prenatal diagnosis of a fetus with Miller-Dieker syndrome]Liangpu Xu, Hailong Huang, Yan Wang, et al.
Journal of Clinical Laboratory Analysis|January 17, 2020
X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestationsMin Zhang, Hailong Huang, Na Lin, et al.
Cellular and Molecular Life Sciences : CMLS|March 6, 2026
Circ_0001428 regulates erythropoiesis and γ-globin expression via activating the ATF4-BCL11A axis in β-thalassemiaJingmin Li, Yali Pan, Meihuan Chen, et al.
Pageof 6