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- A technique already in use is called preimplantation genetic diagnosis (PGD). 目前已经应用的一项技术叫做植入前基因诊断(PGD)。
- Conclution The PCR-DraI method is highly specific,sensitive and suittable for genetic diagnosis of SMA . 结论 PCR DraI酶切法检测适用于SMA的基因诊断
- Conclusion:Single blastomere PCR is stable and reliable,and it can be used for preimplantation genetic diagnosis... 结论建立的单卵裂球PCR技术是稳定可靠的,可以用于单基因病的着床前遗传学诊断。
- Objective:To establish the method of preimplantation genetic diagnosis(PGD) by use of first polar bodies. 目的:建立采用第一极体植入前染色体非整倍体诊断的方法。
- Objective: To establish a genetic diagnosis assay for spinal muscular atrophy (SMA) in children. 摘要目的：建立儿童型脊髓性肌萎缩症(SMA)的特异性基因诊断平台。
- Herein,we briefly describe the latest advances of the research on the genetic diagnosis of monogenetic inherited ... 本文将概述单基因遗传性内分泌代谢病的基因诊断及其临床应用方面的最新研究进展。
- ESHRE preimplantation genetic diagnosis (PGD)consortium:data collection.(May 2000)[J].Human Reprod,2000,15:2673-2680. 徐艳文庄广伦.;荧光原位杂交技术在胚胎植入前性别诊断中的应用[J]
- Conclusion:Single blastomere PCR is stable and reliable,and it can be used for preimplantation genetic diagnosis. 目的建立单卵裂球PCR技术,为开展单基因病的着床前遗传学诊断奠定基础。
- Objectives:This study is to set up a technique of single blastomere PCR,and to provide a basis for preimplantation genetic diagnosis. 目的建立单卵裂球PCR技术,为开展单基因病的着床前遗传学诊断奠定基础。方法共对103个卵裂球进行了PCR扩增;
- Human embryo preimplantation genetic diagnosis (PGD) for sure can solve some problems who have genetic disorder or disease. 人类胚胎着床前遗传学诊断（PGD）能解决诸多有关遗传学异常或疾病的问题。
- The field of this course mainly studies the chromosomal disorder, single gene disorder，polygenetic disorders，genetic diagnosis and counseling. 本课程的五个重要内容包括染色体病、单基因遗传病、多基因遗传病、遗传学诊断与遗传咨询。
- Switzerland genetic testing center located in the scenic Freiburg, is one of the world-renowned center genetic diagnosis. 瑞士基因检测中心坐落于风景优美的弗里堡，是世界知名的基因诊断中心。
- Objective To explore the feasibility of using single cell fluorescent polymerase chain reaction(PCR)in the preimplantation genetic diagnosis(PGD). 目的建立单细胞水平的荧光PCR技术,探讨该技术对临床开展着床前遗传学诊断的可行性。
- Called preimplantation genetic diagnosis, it involves taking a single cell from an embryo when it contains only eight or so cells. 这种称为着床前胚胎遗传学诊断的方法包括从仅含有约8个细胞的胚胎组织中分离单个细胞。
- Conclusion AC2.5 and SM7 are highly polymorphic and can be used in genetic diagnosis of both Chinese Han and Zhuang PKD1 families. 结论AC2.;5和SM7在汉族和壮族中均高度多态(SM7在壮族中稍差)，可用于汉、壮族人PKD1基因诊断。
- Conclusion: PCR-RFLP is sensitive, specific and simple indetecting the deletion of SMN genefor the genetic diagnosis of SMA in children. 结论：应用PCR-RFLP技术对儿童型脊髓性肌萎缩症患儿进行基因诊断具有高度的敏感性和特异性，可作为SMA的诊断方法。
- Objective To investigate the feasibility of multiple displacement amplification(MDA) to apply in the non-invasive prenatal genetic diagnosis of Duchenne muscular dystrophy (DMD). 目的探讨多重置换扩增(multiple displacement amplification,MDA)方法应用到杜氏肌营养不良(Duchenne muscular dystrophy,DMD)的无创性产前基因诊断中的可行性。
- The cytogenetic analysis and the detection of AZF microdeletion on Y chromosome are essential to the final genetic diagnosis to be made for male infertility patients. 通过细胞遗传学检查及 Y染色体上 AZF区域微缺失的检测 ,对男性不育患者提供更加明确的遗传学诊断
- Herein, we briefly describe the latest advances of the research on the genetic diagnosis of monogenetic inherited endocrine and metabolic diseases and its clinical utility. 本文将概述单基因遗传性内分泌代谢病的基因诊断及其临床应用方面的最新研究进展。
- Objective To set up a highly efficient cell lysis system to increase the efficiency of single cell polymerase chain reaction (PCR) for preimplantation genetic diagnosis (PGD). 目的:探讨优化细胞裂解条件,提高植入前诊断中聚合酶链反应的扩增效率。
