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人类染色体上的遗传性脆性位点。III. 在患有X连锁智力障碍的男性及其女性亲属中检测fra(X)(q27)

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives.

作者信息

Sutherland G R

出版信息

Hum Genet. 1979;53(1):23-7. doi: 10.1007/BF00289445.

Abstract

The fragile site at Xq27 which is associated with X-linked retardation with macroorchidism has been studied in 21 retarded males. These males were from 12 families, and studies of nine of the familes were possible. Detection of carrier females is difficult, especially with increasing age. The fragile site was demonstrated in only five of 13 obligate carrier females. It is concluded that using present methods, cytogenetic detection of carriers is fairly reliable in females aged less than 20--25 years but unreliable in older females.

摘要

对21名智力发育迟缓男性进行了研究,他们均存在与X连锁智力发育迟缓伴巨睾症相关的Xq27脆性位点。这些男性来自12个家庭,其中9个家庭的研究得以进行。检测携带者女性很困难,尤其是随着年龄增长。在13名肯定携带者女性中,仅5人检测到了脆性位点。得出的结论是,使用目前的方法,对于年龄小于20 - 25岁的女性,携带者的细胞遗传学检测相当可靠,但对于年龄较大的女性则不可靠。

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