Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30320).

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作者信息

Curtis D, Blank C E

机构信息

Centre for Human Genetics, Sheffield, UK.

出版信息

Hum Genet. 1989 Jan;81(2):200-2. doi: 10.1007/BF00293906.

DOI:10.1007/BF00293906

PMID:2912892

Abstract

摘要

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Am J Ophthalmol. 1984 Mar;97(3):357-65. doi: 10.1016/0002-9394(84)90636-6.

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28.X连锁视网膜色素变性与经重组DNA探针L1.28鉴定的限制性片段长度多态性之间的紧密遗传连锁。

Nature. 1984;309(5965):253-5. doi: 10.1038/309253a0.

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.人类家系中重组率的估计：人类连锁研究似然性的高效计算。

Am J Hum Genet. 1974 Sep;26(5):588-97.

Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.绘制X连锁眼病图谱：II. X连锁视网膜色素变性与X染色体短臂标记的连锁关系。

Hum Genet. 1985;70(1):45-50. doi: 10.1007/BF00389458.

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

Am J Hum Genet. 1987 Oct;41(4):635-44.

Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7.X连锁视网膜色素变性与以下Xp位点的连锁关系分析：L1.28、鸟氨酸转氨甲酰酶（OTC）、754、XJ-1.1、pERT87和C7。

Hum Genet. 1988 Jan;78(1):60-4. doi: 10.1007/BF00291236.

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Hum Genet. 1985;71(2):93-9. doi: 10.1007/BF00283360.

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation.

Hum Genet. 1986 Oct;74(2):168-71. doi: 10.1007/BF00282083.

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