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Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
The Journal of Bone and Joint Surgery. American Volume|November 3, 2022
Autologous Costal Cartilage Grafting for a Large Osteochondral Lesion of the Femoral Head: A 1-Year Single-Arm Study with 2 Additional Years of Follow-upChang-Qing Zhang, Da-Jiang Du, Pei-Chun Hsu, et al.
American Journal of Human Genetics|December 21, 2024
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disordersSheng Luo, Peng-Yu Wang, Peng Zhou, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2026
<i>Chd8</i> haploinsufficiency leads to molecular layer heterotopias and age-dependent cortical expansionFelix A Kyere, Ian Curtin, Ziquan Wei, et al.
Leukemia|April 7, 2019
Prognostic and predictive value of a microRNA signature in adults with T-cell lymphoblastic lymphomaXiao-Peng Tian, Wei-Juan Huang, Hui-Qiang Huang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 3, 2020
A CpG Methylation Classifier to Predict Relapse in Adults with T-Cell Lymphoblastic LymphomaXiao-Peng Tian, Ning Su, Liang Wang, et al.
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