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脆性X连锁智力迟钝基因与凝血因子IX基因之间的连锁和重组

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.

作者信息

Warren S T, Glover T W, Davidson R L, Jagadeeswaran P

出版信息

Hum Genet. 1985;69(1):44-6. doi: 10.1007/BF00295528.

Abstract

Linkage analysis on a family with fragile X-linked mental retardation was performed using a Taq 1 restriction fragment length polymorphism detected by a cloned human coagulation factor IX cDNA. Two affected brothers in this sibship were found to have different factor IX RFLP alleles, indicating a recombinational event occurred between the two genes. Our data therefore indicate that the gene responsible for fragile X-linked mental retardation is not as tightly linked to the factor IX gene as the previously published data may suggest.

摘要

利用克隆的人凝血因子IX cDNA检测到的Taq 1限制性片段长度多态性,对一个患有脆性X连锁智力迟钝的家系进行了连锁分析。在这个同胞关系中,发现两个患病兄弟具有不同的因子IX RFLP等位基因,表明这两个基因之间发生了重组事件。因此,我们的数据表明,导致脆性X连锁智力迟钝的基因与因子IX基因的连锁不像先前发表的数据所显示的那样紧密。

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