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Molecular Biology Reports|August 8, 2024
Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assayFeiyu Zhou, Hongping Zhong, Bo Wu, et al.
American Journal of Medical Genetics. Part A|November 5, 2024
Delayed Diagnosis of Spinal Muscular Atrophy in Two Chinese Families due to Novel SMN1 DeletionsYan Dong, Shuyue Zhang, Hong Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 2024
Identification of novel variants in hereditary spherocytosis patients by whole-exome sequencingLi Qin, Yujiao Jia, Haoxu Wang, et al.
Hepatology (Baltimore, Md.)|December 7, 2018
Hepatic Autophagy Deficiency Compromises Farnesoid X Receptor Functionality and Causes Cholestatic InjuryBilon Khambu, Tiangang Li, Shengmin Yan, et al.
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