Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene.
作者信息
Mercier B, Gaucher C, Mazurier C
机构信息
Laboratoire de Recherche sur l'Hemostase, Centre Regional de Transfusion Sanguine, Lille, France.
出版信息
Nucleic Acids Res. 1991 Sep 11;19(17):4800. doi: 10.1093/nar/19.17.4800.
Abstract
摘要
相似文献
1
Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene.对105名无关个体的F8VWF基因中的98个等位基因进行特征分析。
Nucleic Acids Res. 1991 Sep 11;19(17):4800. doi: 10.1093/nar/19.17.4800.
2
SmaI and HhaI polymorphisms in the 5' region of the human von Willebrand factor gene (F8VWF).人血管性血友病因子基因（F8VWF）5'区域的SmaI和HhaI多态性
Nucleic Acids Res. 1991 Jul 25;19(14):4017. doi: 10.1093/nar/19.14.4017-a.
3
AccI polymorphism in von Willebrand factor (F8VWF) at codon 516.血管性血友病因子（F8VWF）第516密码子处的AccI多态性。
Nucleic Acids Res. 1991 Apr 11;19(7):1729. doi: 10.1093/nar/19.7.1729.
4
An MspI polymorphism in the von Willebrand factor gene.血管性血友病因子基因中的MspI多态性。
Nucleic Acids Res. 1990 Dec 25;18(24):7467. doi: 10.1093/nar/18.24.7467-a.
5
PCR-based detection of a polymorphic HaeIII site in intron VII of the human albumin (ALB) gene.基于聚合酶链反应（PCR）检测人白蛋白（ALB）基因内含子VII中一个多态性HaeIII位点。
Nucleic Acids Res. 1991 Dec 25;19(24):6972. doi: 10.1093/nar/19.24.6972-a.
6
RsaI polymorphism in von Willebrand factor (vWF) at codon 789.血管性血友病因子（vWF）第789位密码子处的RsaI多态性
Nucleic Acids Res. 1990 Aug 25;18(16):4961. doi: 10.1093/nar/18.16.4961-a.
7
AcyI-RFLP in intron 8 of hTPO gene.人甲状腺过氧化物酶（hTPO）基因第8内含子的酰基限制性片段长度多态性
Nucleic Acids Res. 1992 Mar 11;20(5):1162. doi: 10.1093/nar/20.5.1162-a.
8
BstNI/NciI polymorphism of the human p53 gene (TP53).人类p53基因（TP53）的BstNI/NciI多态性
Nucleic Acids Res. 1991 Dec 25;19(24):6969. doi: 10.1093/nar/19.24.6969-a.
9
Hypervariable polymorphism in the APOC3 gene.载脂蛋白C3基因中的高变多态性。
Nucleic Acids Res. 1991 Sep 11;19(17):4799. doi: 10.1093/nar/19.17.4799.
10
A BglII polymorphism in the human NF1 gene.人类NF1基因中的一种BglII多态性。
Nucleic Acids Res. 1991 Sep 11;19(17):4798. doi: 10.1093/nar/19.17.4798.
引用本文的文献
1
Complex variability of intron 40 of the von Willebrand factor (vWF) gene.血管性血友病因子（vWF）基因第40内含子的复杂变异性。
Int J Legal Med. 2008 Jan;122(1):67-71. doi: 10.1007/s00414-006-0149-z. Epub 2007 Feb 2.
2
The STR systems HumVWA and HumACTBP2 in a Hungarian population.
Int J Legal Med. 1996;108(6):316-7. doi: 10.1007/BF02432127.
3
Current management of von Willebrand's disease.血管性血友病的当前治疗方法。
Drugs. 1995 Oct;50(4):602-14. doi: 10.2165/00003495-199550040-00003.
4
Population data and forensic efficiency values for the STR systems HumVWA, HumMBP and HumFABP.
Int J Legal Med. 1994;106(4):183-9. doi: 10.1007/BF01371334.
本文引用的文献
1
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.用于镰状细胞贫血诊断的β-珠蛋白基因组序列的酶促扩增及限制性酶切位点分析。
Science. 1985 Dec 20;230(4732):1350-4. doi: 10.1126/science.2999980.
2
Structure of the gene for human von Willebrand factor.人类血管性血友病因子基因的结构
J Biol Chem. 1989 Nov 25;264(33):19514-27.
3
Tetranucleotide repeat polymorphism in the vWF gene.血管性血友病因子（vWF）基因中的四核苷酸重复多态性
Nucleic Acids Res. 1990 Aug 25;18(16):4957. doi: 10.1093/nar/18.16.4957-a.
4
5
Direct PCR from whole blood, without DNA extraction.无需提取DNA，直接从全血中进行聚合酶链反应。
Nucleic Acids Res. 1990 Oct 11;18(19):5908. doi: 10.1093/nar/18.19.5908.
Zotero 插件