prenatal genetic diagnosis

基本解釋

It provides a new thinking way of non-invasive prenatal genetic diagnosis for single-gene disorders.
為開展其他單基因病的無創(chuàng)性產(chǎn)前遺傳學(xué)診斷研究提供了新的思路。
Objective: To isolate fetal nucleated red blood cells (FNRBCs) from maternal blood, which is used for noninvasive prenatal genetic diagnosis.
目的：從孕婦外周血中分選富集出胎兒有核紅細(xì)胞，以便用于無創(chuàng)傷性產(chǎn)前診斷。
Objective:Fetal nucleated red blood cells(NRBCs) are rare in maternal circulation, but there presence constitutes a potential source of non-invasive prenatal genetic diagnosis.
目的：盡管胎兒有核紅細(xì)胞在母血中含量甚微，但它的存在卻為無創(chuàng)傷性產(chǎn)前基因診斷提供了潛在資源。

Details and clinical data on its new noninvasive prenatal diagnostic test, which detects the genetic roots of Down Syndrome, were just published in the medical journal Prenatal Diagnosis.
FORBES: Aria Diagnostics Emerges From Stealth With New Blood-Based Prenatal Test