一名生殖功能衰竭男性的13/14易位。有丝分裂和减数分裂研究。
13/14 Translocation in a man with reproductive failure. Mitotic and meiotic studies.
作者信息
Mićić M D, Nikolis J G, Mićić S R
出版信息
Hum Genet. 1980;55(1):137-9. doi: 10.1007/BF00329142.
PMID:7450751
Abstract
An inherited (maternal origin) 13/14 translocation with the nucleolus organizer regions eliminated and one centromere was found in an oligospermic man whose wife had had two spontaneous abortions. Meiotic studies revealed all stages of spermatogenesis with a trivalent configuration in diakinesis. Possible reasons for his subfertility and his mother's normal fertility are discussed.
摘要
在一名少精子症男性中发现了一种遗传性（母系起源）13/14易位，核仁组织区缺失且有一个着丝粒，该男性的妻子曾有两次自然流产。减数分裂研究揭示了精子发生的各个阶段，在终变期呈现三价体构型。文中讨论了他生育力低下以及他母亲生育力正常的可能原因。
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