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拟常染色体区域内的缺失有助于定位三个新标记,并表明该区域在线性生长中可能发挥的作用。

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.

作者信息

Henke A, Wapenaar M, van Ommen G J, Maraschio P, Camerino G, Rappold G

机构信息

Institut für Humangenetik, Heidelberg, Germany.

出版信息

Am J Hum Genet. 1991 Oct;49(4):811-9.

Abstract

Short stature is consistently found in individuals with terminal deletions of Xp. In order to refine the localization of a putative locus affecting height, we analyzed two patients with a partial monosomy of the pseudoautosomal region at the molecular level. Eight pseudoautosomal probes were used for the genetic deletion analysis through dose evaluation. Three of them represent new markers (DXS415, DXS419, and DXS406) which were positioned on the pseudoautosomal map by pulsed field gel electrophoresis. Our data suggest that a locus affecting height maps in a region of about 1.5 Mbp, distal to the DXS406 locus and proximal to the DXS415 locus, a region which includes two CpG islands, and rule out an involvement of very distal sequences at the X/Y telomeres.

摘要

身材矮小在Xp末端缺失的个体中一直被发现。为了精确确定一个影响身高的假定基因座的定位,我们在分子水平上分析了两名假性常染色体区域部分单体的患者。通过剂量评估,使用了八个假性常染色体探针进行基因缺失分析。其中三个代表新的标记(DXS415、DXS419和DXS406),它们通过脉冲场凝胶电泳定位在假性常染色体图谱上。我们的数据表明,一个影响身高的基因座位于大约1.5兆碱基对的区域,在DXS406基因座的远端和DXS415基因座的近端,该区域包含两个CpG岛,并排除了X/Y端粒非常远端序列的参与。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6567/1683157/ecbcbb2f15f7/ajhg00081-0124-a.jpg

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