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用于产前细胞遗传学的羊水细胞克隆

Amniocyte clones for prenatal cytogenetics.

作者信息

Hecht F, Peakman D C, Kaiser-McCaw B, Robinson A

出版信息

Am J Med Genet. 1981;10(1):51-4. doi: 10.1002/ajmg.1320100107.

Abstract

Amniotic fluid cells were processed in situ on coverslips in 1,429 consecutive cases from Colorado and Arizona. Two true chromosome mosaics were differentiated from 39 pseudomosaics with clarity by the method described here in detail. The culture failure rate was 1--2% and the error rate was 0% in both laboratories. The time in culture prior to the initial harvest for the last 329 cases was 8.7 days.

摘要

在科罗拉多州和亚利桑那州的1429例连续病例中,羊水细胞在盖玻片上进行原位处理。通过此处详细描述的方法,从39例假性嵌合体中清晰地区分出了2例真正的染色体嵌合体。两个实验室的培养失败率均为1%-2%,错误率均为0%。在最后329例病例中,首次收获前的培养时间为8.7天。

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