首页> 美国卫生研究院文献>American Journal of Human Genetics >Localization of an Ataxia-Telangiectasia Gene to an −500-kb Interval on Chromosome 11q23.1: Linkage Analysis of 176 Families by an International Consortium
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Localization of an Ataxia-Telangiectasia Gene to an −500-kb Interval on Chromosome 11q23.1: Linkage Analysis of 176 Families by an International Consortium

机译:共济失调-毛细血管扩张症基因在染色体11q23.1上的-500-kb间隔的本地化:国际财团对176个家庭的连锁分析。

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摘要

We describe a 20-point linkage analysis map of chromosome 11q22-23 that is based on genotyping 249 families (59 CEPH and 190 A-T). Monte Carlo linkage analyses of 176 ataxia-telangiectasia (A-T) families localizes the major A-T locus to the region between S1819(A4) and S1818(A2). When seven nonlinking families were excluded from subsequent analyses, a 2-lod support interval of ∼500 kb was identified between S1819(A4) and S1294. No recombinants were observed between A-T and markers S384, B7, S535, or S1294. Only 17 of the international consortium families have been assigned to complementation groups. The available evidence favors either a cluster of A-T genes on chromosome 11 or intragenic defects in a single gene.
机译:我们描述了基于基因型249族(59 CEPH和190 A-T)的染色体11q22-23的20点连锁分析图。 176个共济失调-毛细血管扩张(A-T)家族的蒙特卡洛连锁分析将主要的A-T基因座定位在S1819(A4)和S1818(A2)之间的区域。当从随后的分析中排除7个非连接家族时,在S1819(A4)和S1294之间鉴定到2个支持位间隔为〜500 kb。在A-T和标记S384,B7,S535或S1294之间未观察到重组体。国际财团家族中只有17个被分配到了互补组。现有证据支持11号染色体上的A-T基因簇或单个基因中的基因内缺陷。

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