prenatal genetic diagnosis

基本解释

It provides a new thinking way of non-invasive prenatal genetic diagnosis for single-gene disorders.
为开展其他单基因病的无创性产前遗传学诊断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：从孕妇外周血中分选富集出胎儿有核红细胞，以便用于无创伤性产前诊断。
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：尽管胎儿有核红细胞在母血中含量甚微，但它的存在却为无创伤性产前基因诊断提供了潜在资源。

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