Risk calculation in retinitis pigmentosa.
作者信息
Holloway S M, Strain L, Shrimpton A E, Wright A F, Aldred M A, Brosnahan D, Hammer H, Jay M, Brock D J
出版信息
Am J Hum Genet. 1991 Nov;49(5):1094-8.
Abstract
摘要
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本文引用的文献
1
On the heredity of retinitis pigmentosa.关于视网膜色素变性的遗传
Br J Ophthalmol. 1982 Jul;66(7):405-16. doi: 10.1136/bjo.66.7.405.
2
Risk factors for genetic typing and detection in retinitis pigmentosa.视网膜色素变性基因分型与检测的危险因素。
Am J Ophthalmol. 1980 Jun;89(6):763-75. doi: 10.1016/0002-9394(80)90163-4.
3
Easy calculations of lod scores and genetic risks on small computers.在小型计算机上轻松计算连锁分析计分和遗传风险。
Am J Hum Genet. 1984 Mar;36(2):460-5.
4
A strategy to reveal high-frequency RFLPs along the human X chromosome.一种揭示人类X染色体上高频限制性片段长度多态性的策略。
Am J Hum Genet. 1984 May;36(3):546-64.
5
Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus.
Nature. 1985;313(6005):815-7. doi: 10.1038/313815a0.
6
Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27 beta (DXS255).X连锁视网膜色素变性与高变DNA标记M27β（DXS255）的连锁关系。
Hum Genet. 1989 Feb;81(3):283-6. doi: 10.1007/BF00279005.
7
Risk calculations under heterogeneity.异质性下的风险计算
Am J Hum Genet. 1989 Nov;45(5):819-21.
8
Nsi I RFLP at the X-linked chronic granulomatous disease locus (CYBB).位于X连锁慢性肉芽肿病基因座（CYBB）的Nsi I限制性片段长度多态性
Nucleic Acids Res. 1989 May 11;17(9):3619. doi: 10.1093/nar/17.9.3619.
9
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.使用多位点同质性检验定位多个X染色体连锁的视网膜色素变性基因座。
Proc Natl Acad Sci U S A. 1990 Jan;87(2):701-4. doi: 10.1073/pnas.87.2.701.
10
PCR detection of existing and new polymorphism at the TIMP locus.通过聚合酶链反应检测金属蛋白酶组织抑制因子（TIMP）基因座现有的和新的多态性。
Nucleic Acids Res. 1991 Mar 11;19(5):1165. doi: 10.1093/nar/19.5.1165-a.
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