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Plos One|June 21, 2016
Ten Novel Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical Cysts and a Long-Term Follow-Up ResearchBinbin Cao, Huifang Yan, Mangmang Guo, et al.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.International Journal of Genomics|July 31, 2018
Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic LeukodystrophyLi Chen, Huifang Yan, Binbin Cao, et al.Behavioral and Brain Functions : BBF|June 7, 2025
Unraveling genetic risk contributions to nonverbal status in autism spectrum disorder probandsHuan Liu, Shenghan Wang, Binbin Cao, 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.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.Pageof 4