Hasil Pencarian - Fang‐Mei Luo

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  1. 1
    Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding

    Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding oleh Fang-Mei Luo, Fang-Mei Luo, Liang-Liang Fan, Liang-Liang Fan, Yue Sheng, Yi Dong, Lv Liu

    Diterbitkan 2021-06-01
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  2. 2
    Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

    Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A oleh Fang-Mei Luo, Fang-Mei Luo, Ming-Xing Deng, Rong Yu, Lv Liu, Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan

    Diterbitkan 2021-04-01
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  3. 3
    Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

    Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A oleh Fang-Mei Luo, Fang-Mei Luo, Ming-Xing Deng, Rong Yu, Lv Liu, Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan

    Diterbitkan 2021-02-01
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  4. 4
    ZPA Regulatory Sequence Variants in Chinese Patients With Preaxial Polydactyly: Genetic and Clinical Characteristics

    ZPA Regulatory Sequence Variants in Chinese Patients With Preaxial Polydactyly: Genetic and Clinical Characteristics oleh Lei Zeng, Jie-Yuan Jin, Jie-Yuan Jin, Fang-Mei Luo, Fang-Mei Luo, Yue Sheng, Pan-Feng Wu, Pan-Feng Wu, Rong Xiang, Rong Xiang, Rong Xiang, Rong Xiang

    Diterbitkan 2022-05-01
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  5. 5
    A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease

    A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease oleh Liang‐Liang Fan, Lv Liu, Fang‐Mei Luo, Ran Du, Chen‐Yu Wang, Yi Dong, Ji‐Shi Liu

    Diterbitkan 2020-12-01
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  6. 6
    Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

    Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis oleh Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Ai-Qian Zhang, Fang-Mei Luo, Fang-Mei Luo, Yue Sheng, Yue Sheng, Chen-Yu Wang, Chen-Yu Wang, Yi Dong, Yi Dong, Liangliang Fan, Liangliang Fan, Liangliang Fan, Liangliang Fan, Lv Liu

    Diterbitkan 2021-08-01
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  7. 7
    A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly

    A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly oleh Tao Wang, Yu-Xing Liu, Fang-Mei Luo, Yi Dong, Ya-Li Li, Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan

    Diterbitkan 2021-11-01
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  8. 8
    Magnolol alleviates hypoxia-induced pulmonary vascular remodeling through inhibition of phenotypic transformation in pulmonary arterial smooth muscle cells

    Magnolol alleviates hypoxia-induced pulmonary vascular remodeling through inhibition of phenotypic transformation in pulmonary arterial smooth muscle cells oleh Xing-Hua Xiao, Fang-Mei Luo, E.-Li Wang, Min-Yi Fu, Tao Li, Yue-Ping Jiang, Shao Liu, Jun Peng, Bin Liu

    Diterbitkan 2022-06-01
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  9. 9
    GLIS Family Zinc Finger 1 was First Linked With Preaxial Polydactyly I in Humans by Stepwise Genetic Analysis

    GLIS Family Zinc Finger 1 was First Linked With Preaxial Polydactyly I in Humans by Stepwise Genetic Analysis oleh Jie-Yuan Jin, Pan-Feng Wu, Pan-Feng Wu, Fang-Mei Luo, Bing-Bing Guo, Lei Zeng, Lei Zeng, Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan, Ju-Yu Tang, Ju-Yu Tang, Rong Xiang, Rong Xiang, Rong Xiang, Rong Xiang

    Diterbitkan 2022-01-01
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