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ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients 期刊论文
plos one, 2014
Yang, Xiaoling; Gao, Hua; Zhang, Jie; Xu, Xiaojing; Liu, Xiaoyan; Wu, Xiru; Wei, Liping; Zhang, Yuehua
收藏  |  浏览/下载:3/0  |  提交时间:2015/11/10
Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects 期刊论文
GENE, 2014, 卷号: 533, 页码: 565-569
作者:  Zhou Yi[1];  Xie Yingjun[1];  Chen Yongzhen[1];  Zhong Liangying[2];  Shang Meijiao[1]
收藏  |  浏览/下载:4/0  |  提交时间:2019/04/25
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements 期刊论文
HUMAN GENETICS, 2014, 卷号: 133, 期号: 3
作者:  Wang, Feng;  Wang, Hui;  Tuan, Han-Fang;  Nguyen, Duy H.;  Sun, Vincent
收藏  |  浏览/下载:6/0  |  提交时间:2019/12/19
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements 期刊论文
2014, 卷号: 133, 期号: 3, 页码: 331-345
作者:  Wang, Feng;  Wang, Hui;  Tuan, Han-Fang;  Nguyen, Duy H.;  Sun, Vincent
收藏  |  浏览/下载:5/0  |  提交时间:2020/01/13
Genotype-Phenotype Correlations in Severe Acne in a Han Chinese Population 期刊论文
DERMATOLOGY, 2014, 卷号: 229, 期号: 3, 页码: 210-214
作者:  Yang JK;  Wu WJ;  He L[*];  Zhang YP[*]
收藏  |  浏览/下载:18/0  |  提交时间:2015/01/04


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