胚胎植入前的诊断。
染色体易位植入前基因检测能够区分正常和异常染色体的胚胎。
Preimplantation genetic testing for chromosomal translocations is able to distinguish between chromosomally normal and abnormal embryos.
为避免将TSC遗传给下一代，TSC患者可用胚胎植入前遗传学诊断（PGD）技术对体外受精（IVF）形成的胚胎进行TSC基因突变的检测。
People with TSC can consider using pre-implantation genetic diagnosis (PGD) to detect a TSC gene change in embryos created through in vitro fertilization (IVF).
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。
Preimplantation genetic diagnosis is a very early form of prenatal diagnosis aimed at eliminating embryos carrying serious genetic diseases before implantation.
方法应用嵌套式逆转录聚合酶链反应技术检测印记基因p57kip2、LIT1、TSSC3在人类卵母细胞及植入前胚胎的正常表达。
Methods Using nested reverse transcription-PCR to analyze the expression of P57KIP2, LIT1, TSSC3 in human oocytes and preimplantation embryos.
它显示了单细胞测序技术在胚胎植入前基因诊断的临床实践潜力。
It shows the potential of single-cell sequencing technology in preimplantation genetic diagnosis clinical practices.
它显示了单细胞测序技术在胚胎植入前基因诊断的临床实践潜力。
It shows the potential of single-cell sequencing technology in preimplantation genetic diagnosis clinical practices.
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