Conclusion Micro-deletion in AZF gene of Y chromosome is one of the major risks for oligospermatism and azoospermatism. 结论Y染色体AZF微缺失是不明原因无精症、少精症的主要原因之一。
Methods PCR method was used to detect micro-deletion in AZF gene in62 oligospermatism and azoospermatism patients and20 normal male controls. 方法对62例无精症、少精症患者及20例正常男性采用多重聚合酶链反应法进行AZF区基因微缺失检测。
Objective To improve the level of diagnosis in azoospermatism. 目的提高无精子症的诊断水平。
The analysis about genetics pathogenesis for the patient of primary azoospermatism 原发性无精子症患者遗传学病因分析
Methods: By culturing peripheral blood to make up lymphocyte chromosome, we were on going karyotyping of 37 azoospermatism cases. 方法:采用外周血培养对37例无精子症患者进行染色体核型分析。结果:37例无精子症患者中47,XXY8例;
The: To approach the genetics effect and the influence on the assisted reproductive technique, we apply the chromosome analysis for the patients of primary azoospermatism. 目的:应用染色体分析对无精子症患者进行遗传学分析,并探讨其遗传效应及其对辅助生殖技术的影响。