人、鼠新突变疾病的检测。

Molecular biology & medicine Pub Date : 1989-12-01
M Grompe, R A Gibbs, J S Chamberlain, C T Caskey
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引用次数: 0

摘要

分子生物学技术的最新发展极大地促进了检测导致人类和动物遗传疾病的突变的方法。在本文中,我们回顾了这些新方法,并提出了一种诊断算法,有助于常规和快速诊断任何遗传疾病的缺陷基因已被分离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of new mutation disease in man and mouse.

Recent developments in molecular biology technology have greatly facilitated the methods for detection of mutations responsible for genetic disorders in both humans and animals. In this article we review some of these new methods and present a diagnostic algorithm that facilitates the routine and rapid diagnosis of any genetic disorder for which the defective gene has been isolated.

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