Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and DYNC1H1[original query] |
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Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China. Pediatrics and neonatology 2018 Mar . Wang Rongyue, Lei Tingying, Fu Fang, Li Ru, Jing Xiangyi, Yang Xin, Liu Juan, Li Dongzhi, Liao C |
DYNC1H1-related epilepsy: Genotype-phenotype correlation. Developmental medicine and child neurology 2022 9 . Liu Wenwei, Cheng Miaomiao, Zhu Ying, Chen Yi, Yang Ying, Chen Hui, Niu Xueyang, Tian Xiaojuan, Yang Xiaoling, Zhang Yueh |
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- Page last updated:Apr 16, 2024
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