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BMC Medical Genetics|May 16, 2019
Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate geneHuifang Yan, Zhen Shi, Ye Wu, et al.Nano Letters|August 30, 2021
Extrinsic and Intrinsic Anomalous Metallic States in Transition Metal Dichalcogenide Ising SuperconductorsYing Xing, Pu Yang, Jun Ge, et al.Human Molecular Genetics|March 24, 2017
Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disordersLing Zhang, Jingmin Wang, Cheng Zhang, et al.European Journal of Nuclear Medicine and Molecular Imaging|September 23, 2025
Survival effect of PET/CT-defined occult lymph node metastasis in the newly proposed ninth edition N descriptors: a multicentre studyXinchen Shen, Tao Chen, Juemin Yu, et al.Physical Review Letters|June 15, 2024
High-Temperature Anomalous Metal States in Iron-Based Interface SuperconductorsYanan Li, Haiwen Liu, Haoran Ji, et al.Journal of Human Genetics|February 18, 2021
Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencingHuifang Yan, Haoran Ji, Thomas Kubisiak, et al.Neuroscience|September 10, 2021
Novel Insight into the Potential Pathogenicity of Mitochondrial Dysfunction Resulting from PLP1 Duplication Mutations in Patients with Pelizaeus-Merzbacher DiseaseRuoyu Duan, Liuju Li, Huifang Yan, et al.American Journal of Human Genetics|October 8, 2019
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during InfancyHuifang Yan, Guy Helman, Swetha E Murthy, et al.Plos One|February 17, 2018
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patientsHaoran Ji, Dongxiao Li, Ye Wu, et al.Pageof 4