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Burt of the invention, it is provided to check of malformations the chromosomes

机译:本发明的特征在于,提供检查染色体畸形的方法

摘要

A method for antenatal screening for chromosomal abnormalities in which a maternal body fluid from a pregnant women is measured for the level of at least one marker and/or a precursor or metabolite of said marker and the measured level of this marker together with the gestational age of the pregnant woman are compared to reference values at various gestational ages of the level for the marker in (a) pregnant women carrying foetuses having the abnormalitie(s) subject to the screen and (b) pregnant women carrying normal foetuses, the comparison being indicative of the risk of the pregnant woman carrying a foetus with an abnormality subject to the screen characterised in that the level of the marker is affected by maternal age and in making the comparison allowance is made for the age of the pregnant woman.
机译:一种用于染色体异常的产前筛查的方法,其中测量孕妇的母体液中至少一种标志物和/或该标志物的前体或代谢产物的水平,以及该标志物的测量水平以及胎龄在(a)携带受筛查异常的胎儿的孕妇和(b)携带正常胎儿的孕妇中,将孕妇的妊娠率与标记水平在各个胎龄时的参考值进行比较。可以通过筛查来指示孕妇携带胎儿异常的风险,其特征在于,标记物的水平受产妇年龄的影响,并且在比较时考虑了孕妇的年龄。

著录项

  • 公开/公告号DE69418654T2

    专利类型

  • 公开/公告日1999-10-28

    原文格式PDF

  • 申请/专利权人 JOHNSON & JOHNSON CLIN DIAG US;

    申请/专利号DE1994618654T

  • 发明设计人 DAVIES CHRISTOPHER JOHN GB;

    申请日1994-07-19

  • 分类号G01N33/74;

  • 国家 DE

  • 入库时间 2022-08-22 02:11:08

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