Preimplantation genetic diagnosis.
胚胎植入前的诊断。
Objective: To establish a technology of preimplantaion genetic diagnosis.
目的：探索建立植入前遗传学诊断技术。
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)。
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。
Preimplantation genetic diagnosis (PGD) is performed at some centers to screen for inherited diseases.
在有些中心做胚胎植入前遗传诊断(PGD)筛查遗传病。
Objective: To establish the method of preimplantation genetic diagnosis (PGD) by use of first polar bodies.
前言：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。
Nanoscale optical fiber DNA biosensor is designed and prepared, and applied in genetic diagnosis in this article.
本论文研究和制作了纳米光纤dna生物传感器，并将其应用于基因的诊断。
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。
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。
Objective To find out a simple and specific method for genetic diagnosis of hemophilia a and identification of carriers.
目的探索一种更简便和更特异的方法，用于血友病a的基因诊断及其家系遗传咨询。
United application of STR linkage analysis and multiplex allele specific PCR (MASPCR) in PKU genetic diagnosis was also analysed.
同时分析了STR多态性与多重等位基因特异pcr (MASPCR)在PKU基因诊断中的联合应用。
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。
MSPCR and BSPCR were both consistent with genetic diagnosis of PWS. Weight loss surgery is expected to be a major therapy of this disease.
MSPCR和BSPCR相互印证可以作为基因诊断pws的方法，减重手术有望成为此病的主要治疗手段之一。
The molecular genetic research on OSA can assist us in understanding the pathogenesis of OSA and promote genetic diagnosis and prevention of OSA.
对OSA的分子遗传学研究可帮助理解OSA的病因和发病机理，并能促进对OSA的基因诊断和预防。
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。
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).
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。
Then, using a process called pre-implantation genetic diagnosis (PGD), they selected one that was free of the unwanted gene and also matched the boy's tissue type.
之后，通过“移植前基因诊断”，选取了没有病态基因且与孩子组织类型匹配的胚胎。
Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, and explore the clinical significance of genetic diagnosis.
目的探讨婴儿型脊髓性肌萎缩症的临床、电生理特点及基因诊断的临床意义。
Traditionally, the genetic diagnosis of a mendelian disorder relied on the establishment of a clinical diagnosis followed by the sequencing of previously implicated genes.
通常上，孟德尔疾病的遗传诊断主要依靠临床诊断以及随后对疾病已知相关基因的测序。
The technique we use is called pre-implantation genetic diagnosis (PGD), and we're one of the few clinics in South-East Asia with the experience and the facilities to do so.
我们使用的技术被称为胚胎遗传学诊断 （PGD），而我们在东南亚地区的经验和设施，这样做的几个诊所之一。
Dr. Pagan and other researchers say environmental and genetic factors could provide clues for diagnosis, treatments and a cure.
帕甘博士和其他研究人员说，环境和遗传因素能够提供线索，从中找到诊断、治疗和治愈的方法。
But, because your patient had mentioned that he did a Web search you look up the GeneTests site and find some interesting genetic tests that might be useful for the diagnosis.
但是，因为你的病人提到他在网上查阅过资料，所以你也查阅了基因测试网站，并找到了一些可能有助于诊断的有趣的遗传检测方法。
With the jaundice chip, however, diagnosis can be simplified by surveying the genetic code for mutations in specific diseases.
然而有了黄疸芯片后，通过检测特定疾病突变的遗传密码可以很容易的作出诊断。
And it displays the important theories with the practical value on determining genetic sequence, genetic expressing analysis, drugs screening, gene diagnosis and so on.
在基因测序、基因表达分析、药物筛选、基因诊断等领域显示出重要的理论和实用价值。
Researchers have identified TEM1 as a specific genetic marker for the vascular cells associated with tumor growth, a finding that could aid in diagnosis and treatment of ovarian cancer.
最近研究者们发现TEM1可作为与肿瘤生长相关的血管细胞的一个特异性的遗传学标记物，该发现可能有助于卵巢癌的诊断和治疗。
And that will be a boon to medical geneticists, who now often see patients with all the symptoms of a particular disorder but can't verify the diagnosis with a genetic test.
这对基因学家来说无疑是一个喜讯，他们现在经常看到出现有特殊疾病的各种症状，但却不能进行精确的诊断。
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。
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。
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