利用反向点印迹和等位基因特异性PCR分析快速表征b-地中海贫血突变

T. Pavlovic, J. Urosevic, T. Djureinovic, M. D. Janić, L. Krivokapić-Dokmanović
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引用次数: 2

摘要

摘要:本文报告1例重型乙型地中海贫血,应用现代分子遗传学方法对其进行了分子诊断。这个例子展示了我们选择在塞尔维亚共和国检测b-地中海贫血突变的策略,以便在我们的人群中完成分子筛查,并在有风险的怀孕中进行产前诊断。采用RDB(反向点印迹法)和ARMS(扩增难解突变法)对重型地中海贫血患者血液中分离的基因组DNA进行分析。结果表明,该患者是两个b-地中海贫血突变的复合杂合子:b+IVSI-110和b+IVSI-6。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RAPID CHARACTERIZATION OF b-THALASSEMIA MUTATIONS BY REVERSE DOT BLOT AND ALLELE-SPECIFIC PCR ANALYSIS
Summary: This paper reports a case of b-thalassaemia major whose molecular diagnosis was achieved by using modern methods of molecular genetics. This example demonstrates the strategy we chose to detect b-thalassaemia mutations in the Republic of Serbia in order to complete molecular screening in our population and to make prenatal diagnosis in pregnancies at risk. The analysis of genomic DNA isolated from the blood of patient affected with thalassaemia major is carried out by the methods: RDB (reverse dot blot) and ARMS (amplification refractory mutation system). It is shown that the patient is a compound heterozygote for two b-thalassaemic mutations: b+IVSI-110 and b+IVSI-6.
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