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SCNN1B and CA12 play vital roles in occurrence of congenital bilateral absence of vas deferens(CBAVD) 被引量:4
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作者 Ying Shen Huan-Xun Yue +7 位作者 Fu-Ping Li Feng-Yun Hu Xiao-Liang Li Qian Wan Wen-Rui Zhao ji-gang jing Di-Ming Cai Xiao-Hui Jiang 《Asian Journal of Andrology》 SCIE CAS CSCD 2019年第5期525-527,共3页
Dear Editor,Congenital bilateral absence of the vas deferens(CBAVD),a complete or partial defect of the Wolffian duct derivatives,is found in>25% of men with obstructive azoospermia(OA),but the underlying pathologi... Dear Editor,Congenital bilateral absence of the vas deferens(CBAVD),a complete or partial defect of the Wolffian duct derivatives,is found in>25% of men with obstructive azoospermia(OA),but the underlying pathological mechanism remains poorly understood.Previous research has shown that the most common disease associated with CBAVD is cystic fibrosis(CF),the predominant manifestations of which include progressive lung disease,pancreatic dysfunction,elevated sweat chloride electrolyte,meconium ileus,and male infertility. 展开更多
关键词 ELEVATED CBAVD lung
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