Search Results - Jingsi Li

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  1. 441
    Compound heterozygous WDR19 variants associated with nephronophthisis, Caroli disease, refractory epilepsy and congenital bilateral central blindness: Case report

    Compound heterozygous WDR19 variants associated with nephronophthisis, Caroli disease, refractory epilepsy and congenital bilateral central blindness: Case report by Tang, Xianglian, Yi, Sheng, Qin, Zailong, Yi, Shang, Chen, Junjie, Yang, Qi, Li, Shanshan, Luo, Jingsi

    Published in Heliyon
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  2. 442
    Clinical study on 137 cases of unrelated single unit umbilical cord blood hematopoietic stem cell transplantation

    Clinical study on 137 cases of unrelated single unit umbilical cord blood hematopoietic stem cell transplantation by Zhu, Hua, Zhang, Yi, Jin, Huanying, Wang, Yinting, Shao, Xiayan, Kong, Jingsi, Huang, Wenhao, Hong, Yan, Li, Chunli, Gao, Feng, Chen, Liang, Wang, Feng, Lu, Yao

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  3. 443
    Impact of cryopreservation duration of 605 units umbilical cord blood on quality of hematopoietic stem cell and outcome of clinical transplantation

    Impact of cryopreservation duration of 605 units umbilical cord blood on quality of hematopoietic stem cell and outcome of clinical transplantation by Zhang, Yi, Zhu, Hua, Jin, Huanying, Wang, Yinting, Shao, Xiayan, Kong, Jingsi, Huang, Wenhao, Hong, Yan, Li, Chunli, Gao, Feng, Chen, Liang, Wang, Feng, Lu, Yao

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  4. 444
    A synonymous codon variant altering splicing of RBCK1 expands the phenotype and genotype spectra of polyglucosan body myopathy 1

    A synonymous codon variant altering splicing of RBCK1 expands the phenotype and genotype spectra of polyglucosan body myopathy 1 by Wen, Qi, Zhu, Wenjia, Wen, Xinmei, Zhang, Shu, Sun, Yanan, Li, Yun, Wang, Jingsi, Wang, Yaye, Duo, Jianying, Huang, Yue, Lu, Yan, Di, Li, Xu, Min, Wang, Min, Chen, Hai, Da, Yuwei

    Published in Clinical genetics
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  5. 445
    Unusual charge density wave introduced by Janus structure in monolayer vanadium dichalcogenides

    Unusual charge density wave introduced by Janus structure in monolayer vanadium dichalcogenides by Xu, Ziqiang, Shao, Yan, Huang, Chun, Hu, Genyu, Hu, Shihao, Zhi-Lin, Li, Hao, Xiaoyu, Hou, Yanhui, Zhang, Teng, Jin-An, Shi, Liu, Chen, Jia-Ou, Wang, Wu, Zhou, Zhou, Jiadong, Ji, Wei, Qiao, Jingsi, Wu, Xu, Hong-Jun, Gao, Wang, Yeliang

    Published in arXiv.org
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  6. 446
    Image-guided surgery planning for breast reconstruction flap design

    Image-guided surgery planning for breast reconstruction flap design by Huang, Pengfei, Gu, Lixu, Xu, Hua, Dong, Jiasheng, Liu, Jie, Zhang, Jingsi, Song, Jiasi, Yu, Xiao, Chen, Weitao, Zhou, Hongshan, Li, Bowen, Pei, Wei

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  7. 447
    Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism

    Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism by Fu, Chunyun, Chen, Shaoke, Chen, Rongyu, Fan, Xin, Luo, Jingsi, Li, Chuan, Qian, Jiale

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  8. 448
    Deriving phosphorus atomic chain from few-layer black phosphorus

    Deriving phosphorus atomic chain from few-layer black phosphorus by Xiao, Zhangru, Qiao, Jingsi, Lu, Wanglin, Ye, Guojun, Chen, Xianhui, Zhang, Ze, Ji, Wei, Li, Jixue, Jin, Chuanhong

    Published in arXiv.org
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  9. 449
    Case Report: Christianson Syndrome Caused by SLC9A6 Mutation: From Case to Genotype-Phenotype Analysis

    Case Report: Christianson Syndrome Caused by SLC9A6 Mutation: From Case to Genotype-Phenotype Analysis by Lan, Yueyun, Yi, Sheng, Li, Mengting, Wang, Jinqiu, Yang, Qi, Yi, Shang, Chen, Fei, Huang, Limei, Ruan, Yiyan, Shen, Yiping, Luo, Jingsi, Qin, Zailong

    Published in Frontiers in genetics
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  10. 450
    Computer-assisted Preoperative Planning and Surgical Navigation System in Dental Implantology

    Computer-assisted Preoperative Planning and Surgical Navigation System in Dental Implantology by Guangchao Zheng, Lixu Gu, Xiaobo Li, Jingsi Zhang

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  11. 451
    Laparoscopic sphincter-saving surgery for low rectal cancer through marker meeting approach

    Laparoscopic sphincter-saving surgery for low rectal cancer through marker meeting approach by Yang, Xuefei, Zhang, Guixi, Jiang, Li, Zhang, Hao, Liu, Zhihai, Liu, Jingsi, Deng, Yang, Pan, Kai, Man Fan, Joe King

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  12. 452
    Probing Carrier Transport and Structure-property Relationship of Highly Ordered Organic Semiconductors at Two-dimensional Limit

    Probing Carrier Transport and Structure-property Relationship of Highly Ordered Organic Semiconductors at Two-dimensional Limit by Zhang, Yuhan, Qiao, Jingsi, Gao, Si, Hu, Fengrui, He, Daowei, Wu, Bing, Yang, Ziyi, Xu, Bingchen, Li, Yun, Shi, Yi, Ji, Wei, Wang, Peng, Wang, Xiaoyong, Xiao, Min, Xu, Hangxun, Jian-Bin Xu, Wang, Xinran

    Published in arXiv.org
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  13. 453
    Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

    Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature by Su, Jiasun, Fu, Huayu, Xie, Bobo, Lu, Weiliang, Li, Wei, Wei, Yuan, Zhang, Qiang, Wei, Shengkai, Chen, Qiuli, Lu, Yingchi, Jiang, Tingting, Luo, Jingsi, Qin, Zailong

    Published in Molecular cytogenetics
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  14. 454
    A Hybrid Collision Response in a Haptic Virtual Surgery System

    A Hybrid Collision Response in a Haptic Virtual Surgery System by Xiaobo Li, Lixu Gu, Shaoting Zhang, Jingsi Zhang, Guangchao Zheng

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  15. 455
    Mosaic UPD(7q)mat in a patient with silver Russell syndrome

    Mosaic UPD(7q)mat in a patient with silver Russell syndrome by Su, Jiasun, Wang, Jin, Fan, Xin, Fu, Chunyun, Zhang, ShuJie, Zhang, Yue, Qin, Zailong, Li, Hongdou, Luo, Jingsi, Li, Chuan, Jiang, Tingting, Shen, Yiping

    Published in Molecular cytogenetics
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  16. 456
    A minimal invasive surgery simulator employing a novel hybrid cutting method

    A minimal invasive surgery simulator employing a novel hybrid cutting method by Jingsi Zhang, Lixu Gu, Xiaobo Li, Guangchao Zheng, Bo Zhu, Pengfei Huang

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  17. 457
    Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)

    Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3) by Chen, Rongyu, Li, Chuan, Xie, Bobo, Wang, Jin, Fan, Xin, Luo, Jingsi, Hu, Xuyun, Chen, Shaoke, Shen, Yiping

    Published in Molecular cytogenetics
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