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机译:21-羟化酶缺乏症引起的先天性肾上腺增生的基因分型表现为男性不育:病例报告和文献复习
Department of Urology Kyoto University Graduate School of Medicine 54 Shogoin Kawahara-cho Sakyo-ku Kyoto 606-8507 Japan;
Clinical Research Center and The Department of Urology National Hospital Organization Kyoto Medical Center Kyoto Japan;
Department of Urology Kyoto University Graduate School of Medicine 54 Shogoin Kawahara-cho Sakyo-ku Kyoto 606-8507 Japan;
Department of Urology Kyoto University Graduate School of Medicine 54 Shogoin Kawahara-cho Sakyo-ku Kyoto 606-8507 Japan;
Department of Urology Kyoto University Graduate School of Medicine 54 Shogoin Kawahara-cho Sakyo-ku Kyoto 606-8507 Japan;
The Department of Urology National Hospital Organization Kyoto Medical Center Kyoto Japan;
Department of Gynecology Adachi Hospital Kyoto Japan;
Department of Urology Kyoto University Graduate School of Medicine 54 Shogoin Kawahara-cho Sakyo-ku Kyoto 606-8507 Japan;
Clinical Research Center and The Department of Urology National Hospital Organization Kyoto Medical Center Kyoto Japan;
Department of Urology Kyoto University Graduate School of Medicine 54 Shogoin Kawahara-cho Sakyo-ku Kyoto 606-8507 Japan;
21-hydroxylase deficiency; Congenital adrenal hyperplasia; Genotyping; TESE-ICSI;
机译:由于21-羟化酶缺乏症引起的先天性肾上腺增生的基因分型表现为男性不育:病例报告和文献复习。
机译:153名因21羟化酶缺乏症引起的先天性肾上腺皮质增生的基因型与表型的相关性:英国先天性肾上腺皮质增生成人研究执行员(CaHASE)队列的分析
机译:由于21-羟化酶缺乏症,男性迟发性先天性肾上腺皮质增生,可逆且不育,可药用且自发。
机译:先天性肾上腺素增生由于21羟化酶缺乏症的产前诊断和治疗范式
机译:先天性肾上腺皮质增生患儿的肾上腺危机的父母管理。
机译:21-羟化酶缺乏症引起的先天性肾上腺增生的基因分型表现为男性不育:病例报告和文献复习
机译:153名21-羟化酶缺乏症导致的先天性肾上腺皮质增生患者的基因型与表型相关性:英国先天性肾上腺皮质增生成人研究执行员(CaHASE)队列分析