Objective to study the method for gene diagnosis of phenylketonuria.
目的探讨苯丙酮尿症的基因诊断方法。
Results:Gene medication, gene diagnosis and gene therapy were clinical used.
结果基因药物， 基因诊断和治疗已在临床上取得一定应用。
The detection of dynamic mutation is the only way for gene diagnosis of SCA.
检测sca基因的动态突变是目前诊断sca的唯一有效方法。
The PMP22 gene deletion detected by gene diagnosis is the golden criterion for the diagnosis of HNPP.
结论电生理检查对HNPP的诊断很重要，基因检测发现PMP22基因缺失是诊断HNPP的金标准。
This article introduces the gene chip technology and the application in disease gene diagnosis specially.
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。
The thesis focuses on gene diagnosis of diseases, and six new homogenous fluorogenic probes are developed.
绪论部分对现有的几种均相荧光基因探针技术进行了评述，指出了它们所存在的优势与不足。
Objective:To improve the gene diagnosis and carrier detection in for hemophilia A patients and their family members.
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。
SETTING: Gene diagnosis and therapy center in a hospital affiliated to a military medical university of Chinese PLA.
单位：一所军医大学医院基因诊断治疗中心。
This result showed that PCR-SSCP analysis could be effectively used for the direct gene diagnosis of phenylketonuria.
SSCP分析法可有效地用于苯丙酮尿症的基因诊断。
They have great perspective to be used as RNA or DNA treating tools, gene analysis, gene diagnosis, and gene therapy.
它们在用作RNA和DNA工具酶、基因分析和诊断手段以及基因治疗药物等方面的潜力引人注目。
To build China first brand in personalized health management, gene diagnosis and personalized medicine based on genomic medicine.
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。
They have great perspective to be used as RNA or DNA treating tools, gene analysis, gene diagnosis, and gene therapy. The latest d…
它们在用作RNA和DNA工具酶、基因分析和诊断手段以及基因治疗药物等方面的潜力引人注目。
Prenatal gene diagnosis, followed by artificial abortion of affected fetuses, is an effective means of preventing birth of affected babies.
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。
Methods to understand the oncogene which is in relation to hepatocarcinoma and to connect the Medical Imaging with gene diagnosis and therapy.
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。
Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.
目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。
Objectives To study the feature of disease causing mutation of exon 12 of Wilson disease (WD) gene in Chinese and evaluate its value in direct gene diagnosis.
目的研究中国人肝豆状核变性（WD）基因12号外显子的突变特征，为建立直接基因诊断的方法提供理论依据。
Objective:To study the mutations of the phenylalanine hydroxylase(PAH)gene and enhance the gene diagnosis of classical phenylketonuria(PKU) in Inner Mongolia.
目的：研究内蒙古地区经典型苯丙酮尿症（PKU）苯丙氨酸羟化酶（PAH）基因突变的特点和频率，以提高该地区PKU的基因诊断率。
Biochip is an advanced technology for gene sequence determination, gene expression, gene diagnosis, protein function research, high through-put for candidate medicine.
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。
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。
Therefore, the detection of oncogenes and TSGs in different tumors is the basic prerequisite to understand the mechanism of tumorigenesis and to conduct gene diagnosis and gene therapy.
因此，探讨不同类型肿瘤相关癌基因和抑癌基因是认识肿瘤发生分子机理、开展基因诊断和基因治疗的基本前提。
CONCLUSION: Because of the speediness, simpleness and good specificity, the PCR combined with restriction enzyme digestion can be used as a primary screening in the gene diagnosis of CMT1A.
结论：由于PCR -双酶切方法快速、简单、易操作，且特异性好，可作为CMT1A基因诊断的一种初筛方法。
Recent progress in gene engineering and related fields such as gene diagnosis, therapy, bioreactor, protein engineering, metabolism engineering, human genome project, bioinformatics is reviewed.
介绍了基因工程及其在基因检测与基因治疗、生物反应器工程、蛋白质工程与代谢工程，基因组计划与生物信息学等相关领域的进展。
STR and its typing characteristics and applications in genetic map, forensic identification, anthropology, population genetics, gene diagnosis and organ transplantation are reviewed in this paper.
本文介绍了STR及其分型特点，以及STR应用于遗传制图、法医学鉴定、人类学、群体遗传学、基因诊断、器官移植等方面内容。
Objective: To culture and establish Chinese ethnic prostate cancer cell line, investigate its growth characterization and explore experimental methods and models of gene diagnosis and trial of drugs.
目的：培养建立中国人种前列腺癌细胞系，为了解中国人种前列腺癌细胞生长特性、进一步开展前列腺癌基因诊断和药物筛选建立方便的实验手段和模型打下基础。
The gene test was compared to these methods. It improved diagnosis for 16 percent more patients than the leading method, as verified by angiograms they had later.
基因检测与这些方法相比，它比引取方式的诊断率提高了16%，并为后来的血管造影诊断所验证。
The gene test was compared to these methods. It improved diagnosis for 16 percent more patients than the leading method, as verified by angiograms they had later.
基因检测与这些方法相比，它比引取方式的诊断率提高了16%，并为后来的血管造影诊断所验证。
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