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。
Gene mutation analysis is the important tool for genetic counseling and prenatal diagnosis.
基因突变分析是开展遗传咨询和产前诊断的重要工具。
As a codominant genetic marker, restriction fragment length polymorphisms, referred as RFLPs, has been widely Applied to the prenatal diagnosis of some genetic diseases.
限制性酶切片段长度多态性（RFLP）作为共显性的遗传标记，已广泛应用于遗传病的产前诊断。
Preimplantation genetic diagnosis is a very early form of prenatal diagnosis aimed at eliminating embryos carrying serious genetic diseases before implantation.
植入前遗传学诊断作为产前诊断的一种形式，可在胚胎种植前进行诊断，从而防止遗传病的发生。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
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