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    • 72. 发明申请
    • DOWN SYNDROME SCREENING METHOD UTILIZING DRIED BLOOD SAMPLES
    • 使用干燥血液样品的下行综合征筛选方法
    • WO1994003805A1
    • 1994-02-17
    • PCT/US1993007507
    • 1993-08-06
    • MACRI, James, N.
    • G01N33/49
    • G01N33/76Y10S436/817Y10S436/818
    • 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.
    • 本发明涉及通过分析来自孕妇的干血样品来检测产前筛查中的胎儿唐氏综合征(三体21),三体13,三体性18和其他染色体异常的方法。 更具体地说,本发明涉及通过测量游离β人绒毛膜促性腺激素(HCG)的量和游离β(HCG)的切口或断裂或异常形式来改善筛查异常的检测效率的方法,所有这些都是 在本申请中引用作为来自孕妇的干血样品中的游离β(HCG)。