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浏览/检索结果: 共3条，第1-3条 帮助 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 Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens 期刊论文 FERTILITY AND STERILITY, 2015 Yang, Xiaojian; Sun, Qipeng; Yuan, Ping; Liang, Hao; Wu, Xiao; Lai, Luhua; Zhang, Yan 收藏  |  浏览/下载：2/0  |  提交时间：2017/12/03 Congenital absence of vas deferens  CFTR  mutation  variant  CYSTIC-FIBROSIS GENE  BILATERAL ABSENCE  TRANSMEMBRANE REGULATOR  UNILATERAL ABSENCE  FEATURES  CBAVD  MEN  IDENTIFICATION  INFERTILITY  MECHANISMS   Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens 期刊论文 JOURNAL OF CYSTIC FIBROSIS, 2012, 卷号: 11, 页码: 316-323 作者:  Li, Hongjun[1];  Wen, Qiaolian[2];  Li, Hanzhong[1];  Zhao, Lixi[2];  Zhang, Xinyu[1] 收藏  |  浏览/下载：12/0  |  提交时间：2019/04/26 Cystic fibrosis transmetnbrane conductance regulator (CFTR)  Congenital bilateral absence of vas deferens (CBAVD)  Sequencing  Mutation   Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens 期刊论文 2012, 卷号: 11, 期号: 4, 页码: 316-323 作者:  Li, Hongjun;  Wen, Qiaolian;  Li, Hanzhong;  Zhao, Lixi;  Zhang, Xinyu 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 Cystic fibrosis transmetnbrane conductance regulator (CFTR)  Congenital bilateral absence of vas deferens (CBAVD)  Sequencing  Mutation