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Metabolic Brain Disease|April 12, 2017
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes diseaseBinbin Cao, Xiaoping Yang, Yinyin Chen, 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.Orphanet Journal of Rare Diseases|July 20, 2021
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohortDandan Tan, Lin Ge, Yanbin Fan, et al.Clinical Genetics|May 9, 2019
Congenital muscular dystrophies in ChinaLin Ge, Cheng Zhang, Zhaoxia Wang, et al.Pageof 12