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本论丛收集我院遗传研究室82年的论文、简报共十二篇。其中3415例活产婴的核型分析;1168例遗传咨询门诊病人的核型分析,139对流产夫妇的核型分析,提供了我国群体染色体异常发生率和类型的第一手资料。家族性染色体断裂易位热点睾丸决定因子定位的的研究,在细胞遗传学基础理论问题上提出了新的见解。对变化多端的9号染色体有三篇研完报告。另有两篇对 XXY,XX/XY,XX/XXY 两性畸形的病例分析,澄清了过去一些未能解释的问题。此外,还有两篇技术方法的报道。由于每篇文字篇幅简短,未便逐篇分写提要,爰加编者按,综合加以简介。
This essay collects 82 papers in our hospital’s genetic research lab, with 12 articles in brief. Karyotype analysis of 3415 live births; karyotype analysis of 1168 outpatient counseling clinics; and karyotyping of 139 abortion couples, providing first-hand information on the incidence and types of chromosomal abnormalities in our population. Familial chromosomal breakage hot spots testis determinants localization of the basic theory of cytogenetics put forward new ideas. There are three completed reports of the rapidly changing chromosome 9. There are two other cases of XXY, XX / XY, XX / XXY genital abnormalities clarified the past, some problems can not be explained. In addition, there are two technical methods of coverage. As each text space is short, it is inconvenient to write down the summary of each chapter, 爰 plus editors, comprehensive introduction.