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CORC

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TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 7
作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng
收藏  |  浏览/下载：63/0  |  提交时间：2019/12/05
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. 期刊论文
Genetics in medicine : official journal of the American College of Medical Genetics, 2019
作者:  Jiaqi Liu;  Nan Wu;  Nan Yang;  Kazuki Takeda;  Weisheng Chen
收藏  |  浏览/下载：48/0  |  提交时间：2019/12/13
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
Genetics in Medicine, 2019
作者:  Jiaqi Liu;  Nan Wu;  Deciphering Disorders Involving Scoliosis and COmorbidities study, Nan Yang;  Kazuki Takeda;  Weisheng Chen
收藏  |  浏览/下载：40/0  |  提交时间：2019/12/13
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease 期刊论文
2019
作者:  Chen Weisheng;  Lin Jiachen;  Wang Lianlei;  Li Xiaoxin;  Zhao Sen
收藏  |  浏览/下载：32/0  |  提交时间：2020/01/03
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
2019, 卷号: 21, 期号: 7, 页码: 1548-1558
作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng
收藏  |  浏览/下载：34/0  |  提交时间：2020/01/03
Measuring e-service quality and its importance to customer satisfaction and loyalty: an empirical study in a telecom setting 期刊论文
ELECTRONIC COMMERCE RESEARCH, 2019, 卷号: 19, 页码: 477-499
作者:  Zhou, Ronggang;  Wang, Xiaorui;  Shi, Yuhan;  Zhang, Renqian;  Zhang, Leyuan
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/30
考虑资金借贷与资金约束的单产品批量问题 期刊论文
系统工程学报, 2019, 卷号: 34, 页码: 266-276,288
作者:  陈震;  张人千
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/30
Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin alpha 2-related muscular dystrophy 期刊论文
SCIENTIFIC REPORTS, 2018, 卷号: 8
作者:  Ge, Lin;  Liu, Aijie;  Gao, Kai;  Du, Renqian;  Ding, Juan
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/05
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease 期刊论文
HUMAN GENETICS, 2018, 卷号: 137, 期号: 6-7
作者:  Liu, Jiaqi;  Zhou, Yangzhong;  Liu, Sen;  Song, Xiaofei;  Yang, Xin-Zhuang
收藏  |  浏览/下载：22/0  |  提交时间：2019/12/05
枳实含药血清对大鼠胃Cajal间质细胞内质网应激损伤的影响及机制 期刊论文
山东医药, 2018, 卷号: 58, 期号: 41
作者:  王远;  凌江红;  张丽敏;  谭人千;  王煜姣
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05

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