首页> 外国专利> SCREENING METHOD FOR THE DOWN SYNDROME USING DRIED BLOOD SAMPLES

SCREENING METHOD FOR THE DOWN SYNDROME USING DRIED BLOOD SAMPLES

机译:干血样本筛选唐氏综合症的方法

摘要

The present invention relates to a method for detecting fetal Down syndrome (Trisomy 21), trisomy 13, trisomy 18 and other chromosomal anomalies during prenatal screening by analyzing a dried blood sample from a pregnant woman. More particularly the present invention relates to a method for improving detection efficiency in screening for the anomalies by measuring the amount of the free beta human chorionic gonadotropin (HCG) and nicked or fragmented or aberrant forms of free beta (HCG), all of which are referenced throughout this application as free beta (HCG) in dried blood samples from pregnant women.
机译:本发明涉及一种在产前筛查期间通过分析来自孕妇的干血样来检测胎儿唐氏综合症(21三体性),13三体性,18三体性和其他染色体异常的方法。更具体地,本发明涉及一种通过测量游离β人绒毛膜促性腺激素(HCG)和带切口或碎片或异常形式的游离β(HCG)的量来提高筛查异常的检测效率的方法。在整个本申请中将其称为孕妇干血样品中的游离β(HCG)。

著录项

  • 公开/公告号AT230488T

    专利类型

  • 公开/公告日2003-01-15

    原文格式PDF

  • 申请/专利权人 MACRI JAMES N.;

    申请/专利号AT19940906738T

  • 发明设计人 MACRI JAMES N.;

    申请日1993-08-06

  • 分类号G01N33/76;G01N33/68;

  • 国家 AT

  • 入库时间 2022-08-22 00:00:03

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