目的探讨苯丙酮尿症的基因诊断方法。
Objective to study the method for gene diagnosis of phenylketonuria.
结论进行产前基因诊断是预防本病的关键。
Conclusion the key point to prevent the disease is to carry out the antepartum diagnosis.
单位：一所军医大学医院基因诊断治疗中心。
SETTING: Gene diagnosis and therapy center in a hospital affiliated to a military medical university of Chinese PLA.
提示此研究对本病的产前基因诊断具有重要意义。
This result was informative for prenatal diagnosis of the disease.
SSCP分析法可有效地用于苯丙酮尿症的基因诊断。
This result showed that PCR-SSCP analysis could be effectively used for the direct gene diagnosis of phenylketonuria.
结论初步建立了DMD的无创性产前基因诊断的方法。
Conclusion With the use of the method reported, the non invasive prenatal diagnosis of DMD is possible.
目前已经应用的一项技术叫做植入前基因诊断(PGD)。
A technique already in use is called preimplantation genetic diagnosis (PGD).
结果基因药物， 基因诊断和治疗已在临床上取得一定应用。
Results:Gene medication, gene diagnosis and gene therapy were clinical used.
目的探讨人的Y染色体ZFY基因诊断在组织工程中的应用。
Objective To study the diagnosis of ZFY gene on human Y chromosome and its application in tissue engineering.
本文专门介绍了基因芯片技术及其在疾病基因诊断上的应用。
This article introduces the gene chip technology and the application in disease gene diagnosis specially.
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.
方法了解与肝癌有关的癌基因，将影像医学与基因诊断和治疗相结合。
Methods to understand the oncogene which is in relation to hepatocarcinoma and to connect the Medical Imaging with gene diagnosis and therapy.
产前基因诊断，对患病胎儿进行人工流产，是预防患婴出生的有效措施。
Prenatal gene diagnosis, followed by artificial abortion of affected fetuses, is an effective means of preventing birth of affected babies.
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。
Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, and explore the clinical significance of genetic diagnosis.
目的：探讨提高血友病A患者及家系成员的基因诊断、携带者检出的诊断率的途径。
Objective:To improve the gene diagnosis and carrier detection in for hemophilia A patients and their family members.
这也就允许了这些公司可以制造出种种可以垄断多种疾病基因诊断市场的检测方法。
This has permitted firms to create genetic tests that command monopolies over testing for various diseases.
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。
Objective To find out a simple and specific method for genetic diagnosis of hemophilia a and identification of carriers.
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。
And it displays the important theories with the practical value on determining genetic sequence, genetic expressing analysis, drugs screening, gene diagnosis and so on.
生物芯片是基因测序与表达、基因诊断、蛋白功能研究、药物高通量筛选的现代先进技术。
Biochip is an advanced technology for gene sequence determination, gene expression, gene diagnosis, protein function research, high through-put for candidate medicine.
结论肝炎基因诊断芯片可以检测肝组织中HBVDNA，准确率可达75%，假阳性率低。
Conclusion HBVDNA in the liver tissues can be detected by the gene chips, the accuracy of diagnosing was 75% and the rate of the sham positive was lower.
中国最大的以基因组医学为基础的个性化健康管理、基因诊断与个体化用药指导的首选品牌。
To build China first brand in personalized health management, gene diagnosis and personalized medicine based on genomic medicine.
目的：探讨原发性皮肤间变性大细胞淋巴瘤(C - ALCL)临床病理特点和基因诊断方法。
Objective: To explore the clinicopathological features of primary cutaneous anaplastic large cell lymphoma (C-ALCL) and the significance of genetic analysis in the diagnosis.
肝炎基因诊断芯片可以同时检测乙型和丙型肝炎，诊断乙型肝炎血清准确率可达80％，假阳性率低。
Hepatitis B and C can be detected by one gene chip. The accuracy of diagnosing hepatitis B in the serum can reach 80%, the pseudopositive ratio by using gene chips was low.
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。
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。
The molecular genetic research on OSA can assist us in understanding the pathogenesis of OSA and promote genetic diagnosis and prevention of OSA.
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