Hasil Pencarian - Yu'e Chen

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  1. 1
    Toxicokinetic modeling challenges for aquatic nanotoxicology

    Toxicokinetic modeling challenges for aquatic nanotoxicology oleh Wei-Yu eChen

    Diterbitkan 2016-01-01
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  2. 2
    Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study

    Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study oleh Jianlong Zhuang, Na Zhang, Wanyu Fu, Yuying Jiang, Yu’e Chen, Chunnuan Chen

    Diterbitkan 2024-09-01
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  3. 3
    Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study

    Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center ret... oleh Jianlong Zhuang, Na Zhang, Yu’e Chen, Yuying Jiang, Xinying Chen, Wenli Chen, Chunnuan Chen

    Diterbitkan 2024-01-01
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  4. 4
    Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing

    Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing oleh Jianlong Zhuang, Na Zhang, Yu Zheng, Yuying Jiang, Yu’e Chen, Aiping Mao, Chunnuan Chen

    Diterbitkan 2024-04-01
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  5. 5
    Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis‐van Creveld syndrome

    Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis‐van Creveld syndrome oleh Jianlong Zhuang, Shufen Liu, Junyu Wang, Yu'e Chen, Hegan Zhang, Yuying Jiang, Gaoxiong Wang, Chunnuan Chen

    Diterbitkan 2023-10-01
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  6. 6
    Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

    Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication oleh Jianlong Zhuang, Chunnuan Chen, Yuanbai Wang, Shuhong Zeng, Yu’e Chen, Yuying Jiang, Yingjun Xie, Yingjun Xie, Gaoxiong Wang

    Diterbitkan 2022-07-01
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  7. 7
    Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review

    Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review oleh Jianlong Zhuang, Qi Luo, Meihua Xie, Yu’e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen

    Diterbitkan 2023-03-01
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  8. 8
    Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model

    Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model oleh Xiaoyan Lu, Qiman Che, Xinkai Niu, Yilin Zhang, Yu’e Chen, Qing Han, Miaoqing Li, Shuang Wang, Jihong Lan

    Diterbitkan 2023-07-01
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  9. 9
    The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis

    The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis oleh Yu'e Chen, Yingjun Xie, Yingjun Xie, Yuying Jiang, Qi Luo, Lijing Shi, Shuhong Zeng, Jianlong Zhuang, Guorong Lyu

    Diterbitkan 2021-10-01
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  10. 10
    Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing

    Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing oleh Jianlong Zhuang, Chunnuan Chen, Yu'e Chen, Qi Luo, Yuanbai Wang, Yuying Jiang, Shuhong Zeng, Yingjun Xie, Yingjun Xie, Dongmei Chen

    Diterbitkan 2022-04-01
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  11. 11
    Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

    Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing oleh Jianlong Zhuang, Chunnuan Chen, Yu’e Chen, Shuhong Zeng, Yuying Jiang, Yuanbai Wang, Xinying Chen, Yingjun Xie, Yingjun Xie, Gaoxiong Wang

    Diterbitkan 2022-03-01
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  12. 12
    Functional Identification and Characterization of Genes Cloned from Halophyte Seashore Paspalum Conferring Salinity and Cadmium Tolerance

    Functional Identification and Characterization of Genes Cloned from Halophyte Seashore Paspalum Conferring Salinity and Cadmium Tolerance oleh Yu eChen, Chuanming eChen, Zhiqun eTan, Jun eLiu, Lili eZhuang, Zhimin eYang, Bingru eHuang

    Diterbitkan 2016-02-01
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  13. 13
    Effect of different application duration of a venous foot pump on prevention of venous thromboembolism after hip and knee arthroplasty: a multicenter prospective clinical trial

    Effect of different application duration of a venous foot pump on prevention of venous thromboembolism after hip and knee arthroplasty: a multicenter prospective clinical trial oleh Siqi Gu, Yu-e Chen, Mingxing Lei, Jiahui Li, Wanying Li, Meihong Zhang, Hongxia Zhu, Mengying Ma, Dan Kong, Yuan Gao

    Diterbitkan 2023-12-01
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  14. 14
    Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

    Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report oleh Jianlong Zhuang, Junyu Wang, Qi Luo, Shuhong Zeng, Yu’e Chen, Yuying Jiang, Xinying Chen, Yuanbai Wang, Yingjun Xie, Yingjun Xie, Gaoxiong Wang, Chunnuan Chen

    Diterbitkan 2022-08-01
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