A common MspI RFLP of the human fibronectin gene (FN1).
作者信息
Gardella R, Colombi M, Barlati S
机构信息
Division of Biology and Genetics, University of Brescia, Italy.
出版信息
Nucleic Acids Res. 1988 Feb 25;16(4):1651. doi: 10.1093/nar/16.4.1651.
Abstract
摘要
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引用本文的文献
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Human fibronectin gene (FN1) RFLPs: mapping and linkage disequilibrium analysis.人类纤连蛋白基因（FN1）限制性片段长度多态性：定位与连锁不平衡分析。
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Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia.在一个患有隐性营养不良性大疱性表皮松解症和一种小脑共济失调症的家族中，排除基质溶解素-1、基质溶解素-2、间质胶原酶和纤连蛋白基因作为突变位点。
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本文引用的文献
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Human fibronectin: cell specific alternative mRNA splicing generates polypeptide chains differing in the number of internal repeats.人纤连蛋白：细胞特异性可变mRNA剪接产生内部重复序列数量不同的多肽链。
Nucleic Acids Res. 1984 Jul 25;12(14):5853-68. doi: 10.1093/nar/12.14.5853.
2
In situ localization of human fibronectin (FN) genes to chromosome regions 2p14----p16, 2q34----q36, and 11q12.1----q13.5 in germ line cells, but to chromosome 2 sites only in somatic cells.人类纤连蛋白（FN）基因在种系细胞中定位于染色体区域2p14----p16、2q34----q36和11q12.1----q13.5，但在体细胞中仅定位于染色体2的位点。
Cytogenet Cell Genet. 1986;41(1):47-53. doi: 10.1159/000132195.
3
A frequent HaeIII RFLP of the human fibronectin gene.人纤连蛋白基因常见的HaeIII限制性片段长度多态性
Nucleic Acids Res. 1987 Aug 25;15(16):6761. doi: 10.1093/nar/15.16.6761.
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