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CORC

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Cortical thinning and flattening in schizophrenia and their unaffected parents 期刊论文
NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2019, 卷号: 15, 页码: 935-946
作者:  Yan, Jing;  Cui, Yue;  Li, Qianqian;  Tian, Lin;  Liu, Bing
收藏  |  浏览/下载：63/0  |  提交时间：2019/07/12
A novel mutation of the ITGB2 gene in a Chinese Zhuang minority patient with leukocyte adhesion deficiency type 1 and glucose-6-phosphate dehydrogenase deficiency. 期刊论文
Gene, 2019, 卷号: 715
作者:  Zhang Yu;  Yang Xiaotao;  He Xiaoli;  Liu Haifeng;  Guo Pin
收藏  |  浏览/下载：37/0  |  提交时间：2019/12/04
Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia 期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2017, 卷号: 44, 期号: 6, 页码: 295-306
作者:  Tang, Jinsong;  Fan, Yu;  Li, Hong;  Xiang, Qun;  Zhang, Deng-Feng
收藏  |  浏览/下载：58/0  |  提交时间：2017/08/07
Identification of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing 期刊论文
NEUROSCIENCE BULLETIN, 2017
Wen, Zhu; Cheng, Tian-Lin; Yin, Da-Zhi; Sun, Shi-Bang; Wang, Zheng; Yu, Shun-Ying; Zhang, Yi; Qiu, Zilong; Du, Ya-Song
收藏  |  浏览/下载：119/0  |  提交时间：2017/12/03
Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia 期刊论文
Journal of Genetics and Genomics, 2017, 卷号: 44, 期号: X, 页码: 295-306
作者:  Xiang Q;  Zhang DF;  yanqingtang@163.com;  rckchan@psych.ac.cn;  Cwang.cy@163.net
收藏  |  浏览/下载：58/0  |  提交时间：2017/06/26
Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia 期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2017, 卷号: 44, 期号: 6, 页码: 295-306
作者:  Tang Jinsong;  Fan Yu;  Li Hong;  Xiang Qun;  Zhang DengFeng
收藏  |  浏览/下载：9/0  |  提交时间：2021/02/02
Crystal structure and magnetic properties of new Fe3Co3X2 (X = Ti, Nb) intermetallic compounds 期刊论文
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2016, 卷号: 49, 期号: 17, 页码: 1-5
作者:  Zhang, Jie;  Manh Cuong Nguyen;  Balasubramanian, Balamurugan;  Das, Bhaskar;  Sellmyer, David J.
收藏  |  浏览/下载：11/0  |  提交时间：2017/09/13
A novel splice donor site mutation in epha2 caused congenital cataract in a chinese family 期刊论文
Indian journal of ophthalmology, 2016, 卷号: 64, 期号: 5, 页码: 364-368
作者:  Bu, Juan;  He, Sijie;  Wang, Lejin;  Li, Jiankang;  Liu, Jing
收藏  |  浏览/下载：45/0  |  提交时间：2019/05/09
Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism 期刊论文
PLOS ONE, 2015
Li, Jun; Zhao, Linnan; You, Yang; Lu, Tianlan; Jia, Meixiang; Yu, Hao; Ruan, Yanyan; Yue, Weihua; Liu, Jing; Lu, Lin; Zhang, Dai; Wang, Lifang
收藏  |  浏览/下载：6/0  |  提交时间：2017/12/03
湖南人群精神分裂症的遗传易感性研究 学位论文
博士, 北京: 中国科学院研究生院, 2014
作者:  马亮
收藏  |  浏览/下载：22/0  |  提交时间：2014/06/04

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