An EcoRI polymorphism associated with a human genomic clone from band 11p13.
作者信息
Huff V, Compton D, Lewis W, Jones C, Strong L C, Saunders G F
机构信息
Department of Biochemistry, University of Texas System Cancer Center, Houston 77030.
出版信息
Nucleic Acids Res. 1987 Sep 25;15(18):7651. doi: 10.1093/nar/15.18.7651.
Abstract
摘要
相似文献
1
An EcoRI polymorphism associated with a human genomic clone from band 11p13.一种与来自11p13带区的人类基因组克隆相关的EcoRI多态性。
Nucleic Acids Res. 1987 Sep 25;15(18):7651. doi: 10.1093/nar/15.18.7651.
2
Human gastrin (GAS) RFLP recognised by digestion with BamHI or EcoRI.人胃泌素（GAS）经BamHI或EcoRI酶切后可识别的限制性片段长度多态性。
Nucleic Acids Res. 1987 Sep 25;15(18):7652. doi: 10.1093/nar/15.18.7652.
3
BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11.位于11号染色体上胰岛素样生长因子II（IGF2）基因座的BamHI限制性片段长度多态性
Nucleic Acids Res. 1987 Sep 25;15(18):7655. doi: 10.1093/nar/15.18.7655.
4
EcoRI RFLP at 19 cen-q13.2 identified by the anonymous DNA sequence pPM6.7 (D19S18).由匿名DNA序列pPM6.7（D19S18）鉴定的19号染色体cen-q13.2处的EcoRI限制性片段长度多态性
Nucleic Acids Res. 1987 Oct 12;15(19):8120. doi: 10.1093/nar/15.19.8120.
5
pmcf.2-11, a single copy clone from chromosomal region 12q12-q13.1 [D12S32].pmcf.2 - 11，一个来自染色体区域12q12 - q13.1 [D12S32]的单拷贝克隆。
Nucleic Acids Res. 1988 Sep 12;16(17):8749. doi: 10.1093/nar/16.17.8749.
6
An EcoRI polymorphism for pMet G in inbred mice.近交系小鼠中pMet G的EcoRI多态性。
Nucleic Acids Res. 1988 Sep 12;16(17):8745. doi: 10.1093/nar/16.17.8745.
7
Detection of an EcoRI restriction fragment length polymorphism in the gene encoding the human TBP associated factor II 30 (TAF(II)30).人类TBP相关因子II 30（TAF(II)30）编码基因中EcoRI限制性片段长度多态性的检测。
Clin Genet. 1997 Apr;51(4):288-9. doi: 10.1111/j.1399-0004.1997.tb02474.x.
8
A polymorphic locus, D10S5, at 10q21.1.一个位于10q21.1的多态性位点D10S5。
Nucleic Acids Res. 1987 Jul 10;15(13):5498. doi: 10.1093/nar/15.13.5498.
9
A deletion/insertion polymorphism in the human BCR gene on chromosome 22.位于22号染色体上的人类BCR基因中的一个缺失/插入多态性。
Nucleic Acids Res. 1988 Sep 12;16(17):8741. doi: 10.1093/nar/16.17.8741.
10
RFLP of the human c-fes proto-oncogene.人类c-fes原癌基因的限制性片段长度多态性
Nucleic Acids Res. 1988 May 11;16(9):4193. doi: 10.1093/nar/16.9.4193.
引用本文的文献
1
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.无虹膜-威尔姆斯瘤综合征：11号染色体短臂染色体缺失的分子与遗传学分析
Hum Genet. 1989 May;82(2):123-6. doi: 10.1007/BF00284042.
2
Parental origin of de novo constitutional deletions of chromosomal band 11p13.染色体带11p13新发染色体组缺失的亲本来源
Am J Hum Genet. 1990 Jul;47(1):155-60.
3
A panel of restriction fragment length polymorphisms for chromosomal band 11p13.一组针对染色体带11p13的限制性片段长度多态性。
Hum Genet. 1990 Feb;84(3):253-7. doi: 10.1007/BF00200570.
本文引用的文献
1
Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor.家族性无虹膜症与t(4;11)(q22;p13)易位且无肾母细胞瘤
Hum Genet. 1983;63(2):158-61. doi: 10.1007/BF00291536.
Zotero 插件