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家族性微小9号染色体短臂/20号染色体短臂易位:9p24。9p单体综合征的关键片段。

Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.

作者信息

Hoo J J, Fischer A, Fuhrmann W

出版信息

Ann Genet. 1982;25(4):249-52.

PMID:6985017
Abstract

The presence of a chromosomal translocation was suggested in a large kindred with several cases of mental retardation. Chromosome analysis by means of a high resolution technique revealed a translocation of a tiny terminal portion of 9p onto 20p in the presumptive balanced translocation carriers. Five of the affected family members demonstrated monosomy of the terminal portion of 9p. Their clinical features fitted well to the known 9p- syndrome. The breakpoint on 9p is in the distal part of band 9p23. This family confirmed the assumption that the critical segment for monosomy 9p syndrome is located within the terminal band 9p24.

摘要

在一个有几例智力发育迟缓病例的大家族中提示存在染色体易位。通过高分辨率技术进行的染色体分析显示,在推定的平衡易位携带者中,9号染色体短臂(9p)的一小段末端部分易位到了20号染色体短臂(20p)上。5名受影响的家庭成员表现出9号染色体短臂末端部分的单体性。他们的临床特征与已知的9p-综合征非常吻合。9号染色体短臂上的断点位于9p23带的远端部分。这个家族证实了9p单体综合征的关键片段位于9p24末端带内的假设。

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