QQ客服 官方微博 反馈留言

	Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens
	Li, Hongjun[1]; Wen, Qiaolian[2]; Li, Hanzhong[1]; Zhao, Lixi[2]; Zhang, Xinyu[1]; Wang, Jing[2]; Cheng, Longfei[2]; Yang, Jingwen; Chen, Si; Ma, Xu[2,3,4]
刊名	JOURNAL OF CYSTIC FIBROSIS
	2012
卷号	11页码:316-323
关键词	Cystic fibrosis transmetnbrane conductance regulator (CFTR) Congenital bilateral absence of vas deferens (CBAVD) Sequencing Mutation
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/2247103
专题	华南理工大学
作者单位	1.[1]Chinese Acad Med Sci, Dept Urol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China 2.[2]Peking Union Med Coll, Grad Sch, Beijing 100021, Peoples R China 3.[3]Natl Res Inst Family Planning, Ctr Genet, Beijing 100081, Peoples R China 4.[4]World Hlth Org Collaborating Ctr Res Human Reprod, Beijing, Peoples R China
推荐引用方式 GB/T 7714	Li, Hongjun[1],Wen, Qiaolian[2],Li, Hanzhong[1],et al. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens[J]. JOURNAL OF CYSTIC FIBROSIS,2012,11:316-323.
APA	Li, Hongjun[1].,Wen, Qiaolian[2].,Li, Hanzhong[1].,Zhao, Lixi[2].,Zhang, Xinyu[1].,...&Wang, Binbin[2,3].(2012).Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.JOURNAL OF CYSTIC FIBROSIS,11,316-323.
MLA	Li, Hongjun[1],et al."Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens".JOURNAL OF CYSTIC FIBROSIS 11(2012):316-323.

个性服务

查看访问统计

相关权益政策

暂无数据

收藏/分享

除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。