用DNA连接探针诊断妊娠早期囊性纤维化。

Acta Universitatis Carolinae. Medica Pub Date : 1990-01-01
M Németi, Z Papp
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引用次数: 0

摘要

1985年末,囊性纤维化(CF)基因被定位在7号染色体上,7q 22/31。一些限制性片段长度多态性(RFLP)标记与CF基因密切相关。通过对有一个或多个患病儿童的家庭进行研究,通过对绒毛膜绒毛DNA的分析,这些标记物允许对妊娠早期进行准确的产前诊断。在我们的实验室中,13个有CF风险的家庭接受了使用链接DNA探针的建议:xV-2c;pCS.7;满足H;满足D;pJ3.11;19公里。在所有病例中,上述一种或多种探针的信息足以用于妊娠早期产前诊断。在接受检测的13个家庭中,有4个家庭进行了产前诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First trimester diagnosis of cystic fibrosis with linked DNA probes.

In late 1985 the cystic fibrosis (CF) gene was located to chromosome 7, at 7q 22/31. Several restriction fragment length polymorphism (RFLP) markers are closely linked to the CF gene. These markers permit accurate first-trimester prenatal diagnosis based on analysis of chorionic villus DNA by studies of families with one or more affected children. In our laboratory 13 families at risk of having a child with CF have been counselled by the use of linked DNA probes: xV-2c; pCS.7; Met H; Met D; pJ3.11; KM 19. In all cases one or more of the mentioned probes were sufficiently informative to allow first-trimester prenatal diagnosis. In four of the 13 families tested prenatal diagnosis have been performed.

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