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Shanling Liu

Showing results (61-70 of 175) with videos related to

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Pain Physician|May 16, 2023
Comparison of Intercostal Block and Epidural Analgesia for Post-thoracotomy: A Systematic Review and Meta-analysis of Randomized Controlled TrialsZangong Zhou, Xin Zheng, Jianfang Song, et al.
Prenatal Diagnosis|June 29, 2025
Prenatal Phenotype of a Heterozygous Missense CHD4 Variant in a Fetus With Widened Cerebral Subarachnoid Space, Increased Head Circumference and PolyhydramniosFan Zhou, Jing Chen, Shuo Yang, et al.
Orphanet Journal of Rare Diseases|June 11, 2025
Functional characterization of SOX5 variant causing Lamb-Shaffer syndrome and literature review of variants in the SOX5 genePing Wang, Hanbing Xie, Xiao Xiao, et al.
Current Neuropharmacology|June 13, 2025
Mendelian Randomization Uncovers Potential Repurposable Medications for Neuropsychiatric DisordersXiao Xiao, Tingyu Li, Qiang Wang, et al.
Medicine|August 6, 2023
Uncovering a new SASH1 mutation associated with dyschromatosis universalis hereditaria using whole-exome-sequencing: A case reportYue Yang, Nan Jiang, Jing Qun Mai, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|December 16, 2021
L1 Syndrome Prenatal Diagnosis Supplemented by Functional Analysis of One L1CAM Gene Missense VariantPing Wang, Hong Liao, Quyou Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 12, 2018
[Analysis of DYSF gene mutations in two pedigrees affected with limb-girdle muscular dystrophy type 2B]Zhenjun Liu, Hong Liao, Xuemei Zhang, et al.
Prenatal Diagnosis|December 6, 2025
Fetal Phenotype and Diagnosis of Treacher Collins Syndrome Due to a Novel POLR1D VariantXihan Wang, Fenglin Jia, Bo Zhang, et al.
Frontiers in Neuroscience|June 5, 2023
Case report: A novel Cong Zhou, Hongmei Zhu, Qinqin Xiang, et al.
Frontiers in Genetics|December 23, 2025
Early onset Arboleda-Tham syndrome due to <i>KAT6A</i> variants: Case reportHongbo Chen, Dan Yu, Shanling Liu, et al.
Pageof 18

Showing results (61-70 of 175) with videos related to

Sort By:
Pageof 18
Pain Physician|May 16, 2023
Comparison of Intercostal Block and Epidural Analgesia for Post-thoracotomy: A Systematic Review and Meta-analysis of Randomized Controlled TrialsZangong Zhou, Xin Zheng, Jianfang Song, et al.
Prenatal Diagnosis|June 29, 2025
Prenatal Phenotype of a Heterozygous Missense CHD4 Variant in a Fetus With Widened Cerebral Subarachnoid Space, Increased Head Circumference and PolyhydramniosFan Zhou, Jing Chen, Shuo Yang, et al.
Orphanet Journal of Rare Diseases|June 11, 2025
Functional characterization of SOX5 variant causing Lamb-Shaffer syndrome and literature review of variants in the SOX5 genePing Wang, Hanbing Xie, Xiao Xiao, et al.
Current Neuropharmacology|June 13, 2025
Mendelian Randomization Uncovers Potential Repurposable Medications for Neuropsychiatric DisordersXiao Xiao, Tingyu Li, Qiang Wang, et al.
Medicine|August 6, 2023
Uncovering a new SASH1 mutation associated with dyschromatosis universalis hereditaria using whole-exome-sequencing: A case reportYue Yang, Nan Jiang, Jing Qun Mai, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|December 16, 2021
L1 Syndrome Prenatal Diagnosis Supplemented by Functional Analysis of One L1CAM Gene Missense VariantPing Wang, Hong Liao, Quyou Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 12, 2018
[Analysis of DYSF gene mutations in two pedigrees affected with limb-girdle muscular dystrophy type 2B]Zhenjun Liu, Hong Liao, Xuemei Zhang, et al.
Prenatal Diagnosis|December 6, 2025
Fetal Phenotype and Diagnosis of Treacher Collins Syndrome Due to a Novel POLR1D VariantXihan Wang, Fenglin Jia, Bo Zhang, et al.
Frontiers in Neuroscience|June 5, 2023
Case report: A novel Cong Zhou, Hongmei Zhu, Qinqin Xiang, et al.
Frontiers in Genetics|December 23, 2025
Early onset Arboleda-Tham syndrome due to <i>KAT6A</i> variants: Case reportHongbo Chen, Dan Yu, Shanling Liu, et al.
Pageof 18