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A likelihood-based analysis of consistent linkage of a disease locus to two nonsyntenic marker loci: osteogenesis imperfecta versus COL1A1 and COL1A2.

作者信息

Weeks D E

出版信息

Am J Hum Genet. 1990 Sep;47(3):592-4.

PMID:2393031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1683871/
Abstract
摘要

相似文献

1
A likelihood-based analysis of consistent linkage of a disease locus to two nonsyntenic marker loci: osteogenesis imperfecta versus COL1A1 and COL1A2.基于似然性的疾病位点与两个非共线标记位点一致性连锁分析:成骨不全症与COL1A1和COL1A2
Am J Hum Genet. 1990 Sep;47(3):592-4.
2
Strategy for prenatal diagnosis of osteogenesis imperfecta by linkage analysis to the type I collagen loci COL1A1 and COL1A2.通过与I型胶原基因座COL1A1和COL1A2进行连锁分析来进行成骨不全产前诊断的策略。
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Homozygous osteogenesis imperfecta unlinked to collagen I genes.与I型胶原基因无关的纯合子型成骨不全症
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Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.显性遗传的成骨不全症与I型胶原基因座COL1A1和COL1A2的一致连锁关系。
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Osteogenesis imperfecta is linked to both type I collagen structural genes.成骨不全症与I型胶原蛋白结构基因均有关联。
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Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe.成骨不全(IV型)的产前预测:使用胶原蛋白基因探针排除遗传因素
J Med Genet. 1987 Jul;24(7):406-9. doi: 10.1136/jmg.24.7.406.
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Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families.普通人群和成骨不全症家族中I型胶原蛋白基因的单倍型分析。
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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.用于连锁研究的、富集同源基因组区域的强大物理方法:成骨不全症一个基因座的确认
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[Mutation detection of COL1A1 gene in a pedigree with osteogenesis imperfecta].[一个成骨不全家系中COL1A1基因的突变检测]
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本文引用的文献

1
Risk calculations under heterogeneity.异质性下的风险计算
Am J Hum Genet. 1989 Nov;45(5):819-21.
2
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.显性遗传的成骨不全症与I型胶原基因座COL1A1和COL1A2的一致连锁关系。
Am J Hum Genet. 1990 Feb;46(2):293-307.