1号染色体上内部微卫星位点的连锁及恒河猴近端常染色体显性视网膜色素变性的排除
Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.
作者信息
Inglehearn C F, Papiha S S, Jay M, Wright A F, Moore A T, Bhattacharya S S
机构信息
Department of Human Genetics, University of Newcastle upon Tyne.
出版信息
J Med Genet. 1990 Jan;27(1):14-6. doi: 10.1136/jmg.27.1.14.
Abstract
We report the exclusion of a locus for autosomal dominant retinitis pigmentosa proximal to the rhesus locus in a single large pedigree. In addition, a previously unreported linkage is described between two chromosome 1 markers, which confirms that a highly variable minisatellite locus is placed internally on chromosome 1.
摘要
我们报告了在一个大型单一家系中排除了位于恒河猴基因座近端的常染色体显性视网膜色素变性基因座。此外，还描述了两个1号染色体标记之间一种以前未报道过的连锁关系，这证实了一个高度可变的小卫星基因座位于1号染色体内部。
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