Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.
作者信息
Shugart Y Y, Banerjee P, Knowles J A, Lewis C A, Jacobson S G, Matise T C, Penchaszadeh G, Gilliam T C, Ott J
出版信息
Am J Hum Genet. 1995 Aug;57(2):499-502.
Abstract
摘要
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本文引用的文献
1
Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.常染色体显性遗传性视网膜色素变性基因定位于7号染色体长臂。
Nat Genet. 1993 May;4(1):54-8. doi: 10.1038/ng0593-54.
2
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.7号染色体短臂上常染色体显性遗传性视网膜色素变性的一个新基因座。
Nat Genet. 1993 May;4(1):51-3. doi: 10.1038/ng0593-51.
3
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.视网膜色素变性患者中视杆细胞磷酸二酯酶β亚基编码基因的隐性突变。
Nat Genet. 1993 Jun;4(2):130-4. doi: 10.1038/ng0693-130.
4
Faster sequential genetic linkage computations.更快的顺序遗传连锁计算。
Am J Hum Genet. 1993 Jul;53(1):252-63.
5
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.由不连锁的外周蛋白/RDS和ROM1基因座突变引起的双基因视网膜色素变性。
Science. 1994 Jun 10;264(5165):1604-8. doi: 10.1126/science.8202715.
6
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).常染色体显性遗传性视网膜色素变性在7号染色体p臂上的定位（RP9）的进一步细化。
Am J Hum Genet. 1994 Apr;54(4):675-80.
7
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).一张具有厘摩密度的综合性人类连锁图谱。人类连锁合作中心（CHLC）。
Science. 1994 Sep 30;265(5181):2049-54. doi: 10.1126/science.8091227.
8
Avoiding recomputation in linkage analysis.避免连锁分析中的重复计算。
Hum Hered. 1994 Jul-Aug;44(4):225-37. doi: 10.1159/000154222.
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Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.使用专家系统（MultiMap）自动构建遗传连锁图谱：人类基因组连锁图谱。
Nat Genet. 1994 Apr;6(4):384-90. doi: 10.1038/ng0494-384.
10
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19.在19号染色体上鉴定出常染色体显性遗传性视网膜色素变性的第六个基因座。
Hum Mol Genet. 1994 Feb;3(2):351-4. doi: 10.1093/hmg/3.2.351.
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