Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms at two DNA markers, XV-2c and KM. 19, in North African families.
作者信息
Lucotte G, Barré E, David F
出版信息
Am J Hum Genet. 1989 Oct;45(4):635-7.
Abstract
摘要
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本文引用的文献
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Nonuniform recombination within the human beta-globin gene cluster.人类β-珠蛋白基因簇内的不均一重组
Am J Hum Genet. 1984 Nov;36(6):1239-58.
2
Experience with new DNA markers for the diagnosis of cystic fibrosis.
N Engl J Med. 1988 Jan 7;318(1):50-1. doi: 10.1056/NEJM198801073180114.
3
Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis.连锁不平衡数据在囊性纤维化产前诊断中的应用。
Hum Genet. 1988 Sep;80(1):75-7. doi: 10.1007/BF00451460.
4
Cystic fibrosis: typing 89 German families with linked DNA probes.
Hum Genet. 1988 Dec;81(1):54-6. doi: 10.1007/BF00283729.
5
Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families.55个德国家庭中囊性纤维化基因座与两个DNA标记XV2c和KM19的等位基因关联。
Hum Genet. 1988 Sep;80(1):78-80. doi: 10.1007/BF00451461.
6
7
Patterns of polymorphism and linkage disequilibrium for cystic fibrosis.囊性纤维化的多态性和连锁不平衡模式。
Genomics. 1987 Nov;1(3):257-63. doi: 10.1016/0888-7543(87)90052-8.
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Genetic differences between cystic fibrosis with and without meconium ileus.有胎粪性肠梗阻和无胎粪性肠梗阻的囊性纤维化之间的基因差异。
Lancet. 1988 Feb 20;1(8582):376-8. doi: 10.1016/s0140-6736(88)91180-4.
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A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.通过选择无甲基化岛分离出的囊性纤维化位点的一个候选基因。
Nature. 1987;326(6116):840-5. doi: 10.1038/326840a0.
10
Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population.法国人群中，单倍型B（XV - 2c，等位基因1；KM - 19，等位基因2）与囊性纤维化等位基因之间连锁不平衡的确认。
Hum Genet. 1989 Jan;81(2):183-4. doi: 10.1007/BF00293899.
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