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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 11, 2019
[Analysis of co-segregation of methylation pattern and gene ontology among pedigrees affected with neural tube defects]Ruiping Zhang, Jianbo Shu, Linsheng Zhao, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 22, 2020
[Genetic analysis of a child with very long chain acyl-CoA dehydrogenase deficiency]Xiaowei Xu, Xinjie Zhang, Shuxiang Lin, et al.Journal of Attention Disorders|January 3, 2024
Genetic Association of Lipids and Lipid-Lowering Drug Target Genes With Attention Deficit Hyperactivity DisorderDetong Guo, Wenchao Sheng, Yingzi Cai, et al.Frontiers in Pediatrics|August 12, 2022
Case report: Is exchange transfusion a possible treatment for metabolic decompensation in neonates with methylmalonic aciduria in the setting of limited resources?Xiaoyu Cui, Na Li, Hong Xue, et al.BMC Pediatrics|May 31, 2023
Vitamin D metabolic pathway genes polymorphisms and vitamin D levels in association with neonatal hyperbilirubinemia in China: a single-center retrospective cohort studyWeiwei Zhou, Ping Wang, Yanrui Bai, et al.Frontiers in Pediatrics|April 18, 2024
Case Report: A developmental and epileptic encephalopathy 45 due to de novo variant of GABRB1Lu Wang, Haiquan Xu, Jianbo Shu, et al.Global Medical Genetics|January 17, 2024
Novel Variants of CEP152 in a Case of Compound-Heterozygous Inheritance of EpilepsyWeiran Li, Xiaowei Lu, Jianbo Shu, et al.Experimental and Therapeutic Medicine|December 18, 2020
Variants of CAPN3 cause limb-girdle muscular dystrophy type 2A in two Chinese familiesJie Zheng, Xiaowei Xu, Xinjie Zhang, et al.Italian Journal of Pediatrics|November 5, 2020
High-throughput screening reveals novel mutations in spinal muscular atrophy patientsRuiping Zhang, Chunyu Gu, Linjie Pu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 10, 2022
[Analysis of a child with severe combined immunodeficiency due to variants of DCLRE1C gene]Xiaowei Xu, Dandan Yan, Jing Yin, et al.Pageof 8