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Prenatal detection of aneuploidies using fluorescence in situ hybridizaiton: A preliminary experience in an Indian set up

机译:使用荧光原位杂交进行非整倍体的产前检测:在印度建立的初步经验

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摘要

Fluorescence in situ hybridization (FISH) is a powerful molecular cytogenetic technique which allows rapid detection of aneuploidies on interphase cells and metaphase spreads. The aim of the present study was to evaluate FISH as a tool in prenatal diagnosis of aneuploidies in high risk pregnancies in an Indian set up. Prenatal diagnosis was carried out in 88 high-risk pregnancies using FISH and cytogenetic analysis. Multicolour Commercially available FISH probes specific for chromosomes 13, 18, 21, X and Y were used.
机译:荧光原位杂交(FISH)是一种强大的分子细胞遗传学技术,可以快速检测相间细胞和中期扩散上的非整倍性。本研究的目的是评估FISH作为印度机构中高风险妊娠非整倍性产前诊断的工具。使用FISH和细胞遗传学分析对88例高危妊娠进行了产前诊断。多色使用对13、18、21,X和Y染色体具有特异性的市售FISH探针。

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