不孕症夫妇体外受精前进行完整的囊性纤维化病跨膜调节因子基因突变分析的必要性

张剑萍 - 世界核心医学期刊文摘: 妇产科学分册, 2005 - cqvip.com
… analysis of the cystic fibrosis transmembrane regulator (CFTR) gene. Three affected …
mutation screening would be essential if the man has congenital bilateral absence of vas deferens

囊性纤维变性跨膜调节器基因突变对男性生殖的影响

周晨曦, 王曦, 王子栋, 黄宜定 - 中国病理生理杂志, 2001 - cqvip.com
… number of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations
are … of the vas deferens (CBAVD),poor sperm quality, the obstruction and agenesis of the …

先天性双侧输精管缺如伴生精功能障碍一例.

付旭, 周莹, 顾怡栋, 王家雄… - Journal of International …, 2022 - search.ebscohost.com
… [Abstract] The congenital bilateral absence of vas deferens (CBAVD… In addition to the common
mutations of cystic fibrotic … 调节蛋白 (cystic fibrosis transmembrane conductance regulator, …

男性不育与基因缺陷

阮健, 杜卫东 - 遗传, 2010 - chinagene.cn
… 囊性纤 维化跨膜转运调节因子(Cystic fibrosis transmembrane … in men with congenital
bilateral absence of the vas deferens: a … Genetic investigations of CFTR mutations in congenital

人类精子发生中的遗传异常

李宏军 - 发育医学电子杂志, 2019 - fyyxzz.com
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese
patients with congenital bilateral absence of vas deferens … fragmentation in male infertility and …

胰腺炎相关基因多态性的研究进展

张艳冰, 丁佑铭 - 临床肝胆病杂志, 2018 - lcgdbzz.org
… Abstract: Mutations and polymorphisms of genes associated with … , while mutations and
polymorphisms of genes which encode … trypsin inhibitor, cystic fibrosis conductance regulator, …

[HTML][HTML] 不明原因顽固性尿频伴尿失禁诊治经验及文献复习

李中泰, 李彦锋, 张勇, 罗勇, 李珂, 刘旭东, 冯庆兴… - 2018 - aammt.tmmu.edu.cn
… Methods The clinical data of a young man with refractory urinary … 侧输精管缺如(congenital
bilateral absence of the vas deferens,CBAVD),… 其发生与囊性纤维化跨膜转导因子(cystic fibrosis

[PDF][PDF] 2013 年欧洲泌尿科学会男性不育的遗传疾病指南介绍

王万荣, 谭艳, 谢胜, 谢子平, 王澍弘, 欧阳海, 康照鹏 - 2014 - medi-guide.meditool.cn
… 4 囊性纤维化突变和男性不育 囊性纤维化(Cystic fibrosis,CF)是… 缺如(Congenital bilateral
absence of the vas deferens,CBAVD)和… The androgen receptor gene mutations database (ARDB):…

胰腺炎相关基因多态性的研究进展.

丁佑铭, 张艳冰 - Journal of Clinical Hepatology/Linchuang …, 2018 - search.ebscohost.com
… Abstract:Mutations and polymorphisms of genes associated … trypsin inhibitor,cystic fibrosis
conductance regulator,… in Chinese males with congenital bilateral absence of the vas deferens[…

[PDF][PDF] 与囊状纤维化相关的囊状纤维跨膜电导调节因子基因突变体研究进展

徐颢溪 - 蚌埠医学院学报, 2014 - xuebao.bbmc.edu.cn
… of a truncation mutation of the KCNMB3 gene with idiopathic … Clinical practice and genetic
counseling for cystic fibrosismales with congenital bilateral absence of the vas deferens[ J]. …