利用聚合酶链反应（PCR）简便检测凝血因子VIII第19内含子中的HindIII多态性位点 - Suppr

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超能文献

Simple and convenient detection of a HindIII polymorphic site in intron 19 of factor VIII using PCR.

作者信息

Surin V L, Zhukova E L, Krutov A A, Grineva N I

机构信息

Laboratory of Genetic Engineering, All-Union Research Centre for Hematology, Moscow, USSR.

出版信息

Nucleic Acids Res. 1990 Jun 11;18(11):3432. doi: 10.1093/nar/18.11.3432.

DOI:10.1093/nar/18.11.3432

PMID:1972572

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC330987/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18e6/330987/b92685ce8844/nar00195-0284-a.jpg

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Simple and convenient detection of a HindIII polymorphic site in intron 19 of factor VIII using PCR.利用聚合酶链反应（PCR）简便检测凝血因子VIII第19内含子中的HindIII多态性位点

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引用本文的文献

Molecular diagnosis of some common genetic diseases in Russia and the former USSR: present and future.俄罗斯及前苏联一些常见遗传病的分子诊断：现状与未来

J Med Genet. 1993 Feb;30(2):141-6. doi: 10.1136/jmg.30.2.141.

Identification of mutations in two families with sporadic hemophilia A.散发性甲型血友病两个家系中突变的鉴定。

Hum Genet. 1991 Aug;87(4):397-400. doi: 10.1007/BF00197155.

本文引用的文献

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.

Molecular genetics of hemophilia A in man (factor VIII deficiency).人类甲型血友病的分子遗传学（凝血因子 VIII 缺乏症）

Mol Biol Med. 1987 Apr;4(2):81-94.

A new HindIII restriction fragment length polymorphism in the hemophilia A locus.甲型血友病基因座中一种新的HindIII限制性片段长度多态性。

Hum Genet. 1987 Jun;76(2):127-8. doi: 10.1007/BF00284907.

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