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浏览/检索结果: 共7条，第1-7条 帮助 限定条件 发表日期：2017     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Analyzing spatial variations in land use/cover distributions: A case study of Nanchang area, China 期刊论文 ECOLOGICAL INDICATORS, 2017, 卷号: 76, 页码: 52-63 作者:  Zhang, Yang;  Wang, Chuansheng;  Xie, Hongbin;  Zhang, Jie;  Wu, Jiaping 收藏  |  浏览/下载：27/0  |  提交时间：2019/09/25 Spatial pattern  Landscape  Gradient  Density indicator  Scale effect   Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: Pooled results from two Chinese genome-wide association studies 期刊论文 Gut, 2017, 卷号: 66, 期号: 4 作者:  Wang, Zhaoming/35346086300[0];  Dai, Juncheng/56892491500[1];  Hu, Nan/57054892400[2];  Miao, Xiaoping/57054924800[3];  Abnet, Christian C./6701628811[4] 收藏  |  浏览/下载：35/0  |  提交时间：2019/12/05 Estimation of heritability for nine common cancers using data from genome-wide association studies in Chinese population 期刊论文 INTERNATIONAL JOURNAL OF CANCER, 2017, 卷号: 140, 期号: 2 作者:  Dai, Juncheng;  Shen, Wei;  Wen, Wanqing;  Chang, Jiang;  Wang, Tongmin 收藏  |  浏览/下载：15/0  |  提交时间：2019/12/05 cancer  heritability  single-nucleotide polymorphisms  Chinese population  genome-wide complex trait analysis   Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation 期刊论文 BMC MEDICAL GENETICS, 2017 Zhang, Qingping; Wang, Jiaping; Li, Jiarui; Bao, Xinhua; Zhao, Ying; Zhang, Xiaoying; Wei, Liping; Wu, Xiru 收藏  |  浏览/下载：7/0  |  提交时间：2017/12/03 FOXG1  RTT  RTT-like MR  Epilepsy  Hypoplasia of corpus callosum  VARIANT  MOSAICISM  DISORDER  CRITERIA  EPILEPSY  MECP2   SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures 期刊论文 BMC MEDICAL GENETICS, 2017 Wang, Jiaping; Gao, Hua; Bao, Xinhua; Zhang, Qingping; Li, Jiarui; Wei, Liping; Wu, Xiru; Chen, Yan; Yu, Shujie 收藏  |  浏览/下载：5/0  |  提交时间：2017/12/03 SCN8A  Epileptic encephalopathy  Family cases  DE-NOVO MUTATIONS  SODIUM-CHANNEL  PHENOTYPIC SPECTRUM  CLINICAL SPECTRUM  SCN2A MUTATIONS  RECURRENT  NA(V)1.6  CHILDREN   Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies 期刊论文 2017, 卷号: 66, 期号: 4, 页码: 581-587 作者:  Wang, Zhaoming;  Dai, Juncheng;  Hu, Nan;  Miao, Xiaoping;  Abnet, Christian C. 收藏  |  浏览/下载：12/0  |  提交时间：2020/01/03 Estimation of heritability for nine common cancers using data from genome-wide association studies in Chinese population 期刊论文 2017, 卷号: 140, 期号: 2, 页码: 329-336 作者:  Dai, Juncheng;  Shen, Wei;  Wen, Wanqing;  Chang, Jiang;  Wang, Tongmin 收藏  |  浏览/下载：5/0  |  提交时间：2020/01/03 cancer  heritability  single-nucleotide polymorphisms  Chinese population  genome-wide complex trait analysis