探寻与高功能孤独症和Asperger综合征相关的拷贝数变异
序号 | 标题 | 类型 | 作者 |
---|---|---|---|
1 | MeCP2与神经发育性疾病 | 期刊论文 | 何艳琴|公晓红|张宏丽|王红艳|杨章民|HE Yan-Qin 1,2,GONG Xiao-Hong 2,ZHANG Hong-Li 1, W|2 School of Life Sciences,Fudan University,Shangha| |
2 | Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population | 期刊论文 | Liu yanyan|Du yasong|Liu wenwen|Yang caohua|Liu yan|Wang hongyan|Gong xiaohong| |
3 | The genetic variation of CCR5, CXCR4 and SDF-1 in three Chinese ethnic populations | 期刊论文 | Liu, Yanyan|Liu, Feng-Liang|He, Yanqin|Li, Liming|Li, Shilin|Zheng, Yong-Tang|Wang, Hongyan|Gong, Xiaohong| |
4 | High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability | 期刊论文 | Gong, Xiaohong|Gao, Xuewu|Shen, Yiping|Wu, Xiru|Qiu, Zilong|Jin, Li|Wu, Bai-Lin|Wang, Hongyan|Jiang, Yu-wu|Zhang, Xin|An, Yu|Zhang, Jun|Wu, Ye|Wang, Jingmin|Sun, Yangfei|Liu, Yanyan| |