1) preimplantation genetic diagnosis
植入前遗传学诊断
1.
Progress in research on the preimplantation genetic diagnosis for Duchenne muscular dystrophy;
Duchenne型肌营养不良症植入前遗传学诊断研究进展
2.
ObjectiveTo detect two exons of Duchenne muscular dystrophy (DMD) gene and a gender discrimination locus amelogenin gene by single cell triplex PCR, and to evaluate the possibility of this technique for preimplantation genetic diagnosis (PGD) in DMD family with DMD deletion mutation.
目的:采用三重PCR技术检测缺失型杜氏肌营养不良(Duchenne muscular dystrophy,DMD)基因部分外显子和性别鉴定位点amelogenin基因,探讨该技术对DMD家系中致病基因携带者进行植入前遗传学诊断(preimplantation genetic diagnosis,PGD)的可行性。
3.
Objective To investigate the feasibility and risk of preimplantation genetic diagnosis (PGD) for screening normal offspring of Robertsonian translocation carriers.
目的 探讨植入前遗传学诊断 (preimplantation genetic diagnosis,PGD)用于筛选罗伯逊易位携带者无遗传缺陷后代的可行性及风险。
3) Preimplantation genetic diagnosis
胚胎植入前遗传学诊断
1.
Advances in preimplantation genetic diagnosis for chromosomal translocation carrier;
染色体易位携带者的胚胎植入前遗传学诊断研究进展
4) Pre-implantation Genetic Diagnosis(PGD)
植入前遗传学诊断(PGD)
1.
Ethical Thinking on Pre-implantation Genetic Diagnosis(PGD)
胚胎植入前遗传学诊断(PGD)的伦理思考
5) preimplantation genetic diagnosis
植入前诊断
1.
Single cell PCR for sex determination in preimplantation genetic diagnosis;
运用单细胞聚合酶链式反应进行植入前诊断的性别鉴定
2.
Comparison of different lysis buffers in the assessment of the efficiency of single cell polymerase chain reaction for preimplantation genetic diagnosis;
细胞裂解法对植入前诊断中聚合酶链反应扩增效率的影响
3.
To develop a rapid,high efficient,reliable method for preimplantation genetic diagnosis of 21 trisomy syndrome,fluorescence quantitative PCR method was used to detect the original copies of Down syndrome by amplifying the critical region gene(DSCR3) and house-keeping gene GAPDH.
探讨建立一个高效、稳定的21三体遗传病植入前诊断的方法,以染色体G显带核型分析为对照,取正常成人外周血单个淋巴细胞40枚、21三体患者外周血单个淋巴细胞40枚及单卵裂球20枚,采用荧光定量PCR技术同时扩增21号染色体上特异区域基因片段(DSCR)和12号染色体上管家基因(GAPDH)片断作内对照,结果在正常组织同时扩增二片断的有效率为95%(38/40),扩增产物的荧光强度比值为1。
6) Preimplantation diagnosis
植入前诊断
补充资料：胚胎植入前诊断
胚胎植入前诊断
随着体外受精、配子与胚胎显微操作技术和基因超微量分析技术的发展，从宫腔灌洗液或体外受精方法获取胚胎。通过极体活检，卵裂球活检，胚泡活检等技术取样，采取DNA诊断以及蛋白与酶代谢测定，诊断某些遗传病，如囊性纤维化病，Duchcnne型肌营养不良、甲型血友病、脆性综合征和TaySacy病等。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条