Hasil Pencarian - Liangshan Li

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  1. 1
    A Novel Homozygous VPS13B Splice-Site Mutation Causing the Skipping of Exon 38 in a Chinese Family With Cohen Syndrome

    A Novel Homozygous VPS13B Splice-Site Mutation Causing the Skipping of Exon 38 in a Chinese Family With Cohen Syndrome oleh Liangshan Li, Liangshan Li, Xiangmao Bu, Yuhua Ji, Ping Tan, Shiguo Liu

    Diterbitkan 2021-04-01
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  2. 2
    Pressure Relief and Bolt Grouting Reinforcement and Width Optimization of Narrow Coal Pillar for Goaf-Side Entry Driving in Deep Thick Coal Seam: A Case Study

    Pressure Relief and Bolt Grouting Reinforcement and Width Optimization of Narrow Coal Pillar for Goaf-Side Entry Driving in Deep Thick Coal Seam: A Case Study oleh Liangshan Li, Deyu Qian, Xingguo Yang, Hexi Jiao

    Diterbitkan 2022-10-01
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  3. 3
    Two Chinese siblings of combined oxidative phosphorylation deficiency 14 caused by compound heterozygous variants in FARS2

    Two Chinese siblings of combined oxidative phosphorylation deficiency 14 caused by compound heterozygous variants in FARS2 oleh Liangshan Li, Jianhua Ma, Jingli Wang, Liping Dong, Shiguo Liu

    Diterbitkan 2022-09-01
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  4. 4
    Is 18F-PET-CT the First Choice for Preoperative Screening 
for Ia Non-small Cell Lung Cancer?

    Is 18F-PET-CT the First Choice for Preoperative Screening 
for Ia Non-small Cell Lung Cancer? oleh Chuang HE, Jing YUAN, Yuxiao CHEN, Li YANG, Liangshan LI, Tingyuan LI, Xuequan HUANG

    Diterbitkan 2018-07-01
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  5. 5
    Photocatalytic Activation of Saturated C–H Bond Over the CdS Mixed-Phase Under Visible Light Irradiation

    Photocatalytic Activation of Saturated C–H Bond Over the CdS Mixed-Phase Under Visible Light Irradiation oleh Houde She, Liangshan Li, Hua Zhou, Lei Wang, Jingwei Huang, Qizhao Wang, Qizhao Wang

    Diterbitkan 2018-10-01
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  6. 6
    Targeted regions sequencing identified four novel PNPLA1 mutations in two Chinese families with autosomal recessive congenital ichthyosis

    Targeted regions sequencing identified four novel PNPLA1 mutations in two Chinese families with autosomal recessive congenital ichthyosis oleh Liangshan Li, Wenmiao Liu, Yinglei Xu, Miaomiao Li, Qian Tang, Bo Yu, Renmei Cai, Shiguo Liu

    Diterbitkan 2020-02-01
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  7. 7
    Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report

    Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report oleh Xianghong Li, Liangshan Li, Yaqi Sun, Fuyan Lv, Guoqing Zhang, Wenmiao Liu, Meiyan Zhang, Hong Jiang, Shiguo Liu

    Diterbitkan 2019-08-01
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