聚合酶链反应检测D4S43处的双等位基因多态性。 - Suppr

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超能文献

PCR detection of a biallelic polymorphism at D4S43.

作者信息

Majer M, Gerdes B, Zühlke C, Thies U

机构信息

Institut für Humangenetik, Universität Göttingen, FRG.

出版信息

Nucleic Acids Res. 1992 Feb 25;20(4):926. doi: 10.1093/nar/20.4.926.

DOI:10.1093/nar/20.4.926

PMID:1542595

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC312056/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1503/312056/90c158d2ad67/nar00078-0271-a.jpg

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本文引用的文献

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.一种通过分析扩增的DNA序列进行遗传性疾病产前诊断的改进方法。应用于甲型血友病。

N Engl J Med. 1987 Oct 15;317(16):985-90. doi: 10.1056/NEJM198710153171603.

Clustering of multiallele DNA markers near the Huntington's disease gene.亨廷顿舞蹈症基因附近多等位基因DNA标记的聚类

J Clin Invest. 1989 Sep;84(3):1013-6. doi: 10.1172/JCI114222.

Detection by PCR of a VNTR polymorphism at D4S43.通过聚合酶链反应（PCR）检测D4S43处的可变数目串联重复序列（VNTR）多态性。

Nucleic Acids Res. 1991 Sep 11;19(17):4772. doi: 10.1093/nar/19.17.4772.

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