产前诊断
- 网络prenatal diagnosis;prenataldiagnosis
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结论羊水细胞培养进行产前诊断是十分安全而可靠的。
Conclusion amniotic fluid culture for prenatal diagnosis is very safe and reliable .
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从母血浆提取胎儿DNA行产前诊断的研究
Study of Detecting Fetal DNA from Mutual plasma for Prenatal Diagnosis
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循环胎儿DNA及其在产前诊断中的应用
Detection of circulating fetal DNA in maternal plasma and its application in prenatal diagnosis
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脆性X综合征的基因诊断与产前诊断
Genetic Diagnosis and Prenatal Genetic Diagnosis of Fragile X Syndrome
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X染色体倒位伴X连锁无汗性外胚叶发育不良一个家系的产前诊断
Prenatal diagnosis of X-linked anhidrotic ectodermal dysplasia with X-chromosome inversion
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孕妇外周血中胎儿游离DNA的发现,为无创性产前诊断开辟了一条新途径。
The discovery of circulating fetal DNA paves a new way for non-invasive prenatal diagnosis .
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同源基因定量PCR方法快速产前诊断Down综合征
Rapid prenatal detection of Down syndrome by homologous gene quantitative PCR
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应用PCR和斑点杂交产前诊断α&地中海贫血
Prenatal Diagnosis of α - Thalassemia by PCR and Southern Blot
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FISH技术在快速产前诊断中应用的研究
The Research of FISH in Rapid Prenatal Diagnosis
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地高辛素标记弓形虫DNA探针的制备及在产前诊断的应用
Preparation of Digoxigenin-labeled DNA Probe and its Application to Detection of Toxoplasma gondii in Pregnant Women
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应用DNA多态性进行β-地中海贫血产前诊断的可行性
A Study on Feasibility of Prenatal Diagnosis of β - Thalassemia by DNA Polymorphisms in Chinese
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长距离PCR在血友病A携带者检测和产前诊断中的应用
Application of long distance-PCR to hemophilia A carrier detection and prenatal diagnosis
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孕妇血浆中游离胎儿DNA可以用于无创伤产前诊断。
Fetal DNA in maternal plasma could be regarded as the gene resource for noninvasive prenatal diagnosis .
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血浆DNA甲基化的分析进一步应用于无创性产前诊断具有可行性。
The analysis of DNA methylation in plasma will have the powerful potentiality that applicate to noninvasive prenatal diagnosis .
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应用磁激活细胞分选法从母血中分离胎儿有核红细胞做FISH行无创性产前诊断的研究
Non-invasive Prenatal Diagnosis From Maternal Blood : FISH of Fetal Nucleated Erythrocytes Isolated by Magnetic Activated Cell Sorting
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结论FISH技术用于产前诊断孕早期胚胎染色体数目异常具有快速、准确等优点。
Conclusion : FISH technique applied in prenatal diagnosis of early embryo chromosomes abnormalities is rapid and accurate .
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方法:对342例具有产前诊断指征高风险孕妇抽取孕中期羊水细胞培养,制备中期细胞染色体,G显带分析。
Methods Amniocentesis was employed to detect amniotic cells collected from 342 pregnant women with high-risk prenatal diagnosis indications .
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对一血友病a(ha)家系进行携带者及产前诊断。
To make the carrier detection and prenatal diagnosis in a pedigree with hemophilia A.
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TORCH感染介入性产前诊断195例分析
Analysis of 195 cases of invasive prenatal diagnosis for TORCH infections
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甲型血友病产前诊断&应用DNA聚合酶链反应(PCR)进行家系RFLP连锁分析
The Prenatal Diagnosis of Hemophilia A & The Use of PCR and Family RFLP Analysis
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结论胎儿DNA随着孕周的增加而增长,母体血浆是进行无创性产前诊断的非常有价值的底物。
Conclusions The concentration of fetal DNA increases with the progress of pregnancy . Maternal plasma may be valuable in noninvasive prenatal diagnosis .
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FISH技术在遗传病诊断及产前诊断中的应用
The Application of Fluorescence in Situ Hybridization Technology ( FISH ) to the Diagnosis of Chromosome Abnormality in Genetic Diseases and Prenatal Diagnosis
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超声影像技术对HbBart's水肿胎早期产前诊断的研究
Research of early prenatal diagnosis to Hb Bart 's hydrops fetus by ultrasonography
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结论应用孕妇血浆中胎儿DNA作产前诊断敏感性和特异性较高,是一种无创性产前基因诊断方法,具有广泛的临床应用前景。
Conclusions Detecting fetal DNA in maternal plasma is a non-invasive prenatal gene diagnosis with high sensitivity and specificity and is very promising in clinical practice .
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目的建立一种非创伤性的取材和快速胎儿性别诊断方法,并应用于X连锁遗传病的产前诊断。
Objective To find a way of sampling without any wound and quick diagnosis of fetal sex and its application in X-linked recessive inheritance .
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我们体会DNA体外PCR扩增结合寡核苷酸探针点杂交方法可用于PKU的产前诊断和携带者检出。
PCR amplification combining with oligonucleotide dot hybridization is technically feasible for prenatal diagnosis and carrier screening for PKU .
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超声心动图对胎儿先天性心脏病产前诊断价值的Meta分析
Meta-analysis of the value of fetal echocardiography for the prenatal diagnosis of congenital heart disease
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应用聚合酶链式反应体外DNA放大和同位素或非同位素标记的探针在我国南方进行了β地中海贫血的产前诊断。
A prenatal diagnosis of β thalassemia was carried out in South China using a in vitro DNA amplification by a polymerase chain reaction and isotope-labeled or nonradioactive probes .
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母子ABO血型不合的产前诊断
Antepartum diagnosis of maternal-fetal blood group ABO incompatibility
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羊水CK、LDH、Mb联合检测进行DMD产前诊断的临床研究
Clinical research of DMD prenatal dignosis , using determining amniotic fluid CK , LDH and Mb