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.
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.
‘对这些基因作进一步的分析，了解它们如何影响大脑的发育，可能会帮助我们找到更好的方法来诊断和治疗孤独症儿童。’
Detailed analysis of the genes and how they affect brain development is likely to yield better strategies for diagnosing and treating children with autism.
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.
BRCA1和BRCA2基因的发现，为乳腺癌的预防、诊断和治疗带来新的技术方法，还降低了乳腺癌治疗的风险。
Identifying BRCA1 and BRCA2 has led to new techniques for lowering, detecting, and treating breast cancer, and lowering the risk for the disease.
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。
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.
癌症研究团队英国方面的癌症信息主任莱斯利·沃克说，“这是一项激动人心的研究，增进了我们对于p53基因机理的了解。揭示它是怎样起调节作用的，对研发更有效的药品和癌症诊断方法有重要的意义。”
Lesley Walker, cancer Research UK's director of cancer information, said: "This is a really exciting study which improves our understanding of how the p53 gene works."
检测sca基因的动态突变是目前诊断sca的唯一有效方法。
The detection of dynamic mutation is the only way for gene diagnosis of SCA.
方法用反向点杂交法(rdb)诊断患儿的基因突变点。
Methods the gene mutations were diagnosed by the reverse dot blot (RDB).
用于诊断流感A病毒的H5和N1基因的存在的寡核苷酸，其用途，检测方法和试剂盒。
Oligonucleotides, use thereof, detecting method and kit for diagnosing the presence of H5 and N1 genes of the influenza a virus.
本文针对基于SVM的多病类诊断基因选择方法进行了研究。
The methods of diagnostic gene selection for multi-class diseases based on SVM are studied in this paper.
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.
结论红细胞冷冻断裂电镜技术可作为诊断dmd的辅助检查手段，也可作为检测d MD基因携带者的一种方法。
Conclusion The erythrocyte freeze-fracture electron microscopic technology may serve as a method for accessory examination of diagnosing DMD patients and a method for detecting DMD carriers.
本试验以EMA - 1基因重组蛋白为诊断抗原，用EL IS A方法对延边地区马巴贝斯虫病进行了血清学调查。
Babesiosis equi serum epidemiology investigations in yanbian area were using the EMA-1 genetic recombinant protein as diagnosis antigen by the ELISA.
目的建立一种快速、特异、敏感的诊断方法，对痢疾杆菌的致病基因进行基因检测研究。
Objective To establish a speed convenient and susceptive diagnosed method by detecting the invasion associated genes of shigella.
基因芯片、蛋白质组学和免疫组学等研究方法已成为目前卵巢癌早期诊断研究的热点，但尚无确切定论。
Gene chips, proteomics and immunohistochemical tecnology and other research methods have become research hotspot in early diagnosis of ovarian cancer, but there is no definite conclusion.
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。
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.
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。
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.
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。
MSPCR and BSPCR were both consistent with genetic diagnosis of PWS. Weight loss surgery is expected to be a major therapy of this disease.
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.
目的：建立对男性无精症病人YRRM1的基因缺失诊断方法。
Objective: In order to establish a method to detect the abnormal YRRM1 gene in azoospermia.
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.
建立乙型肝炎病毒变异基因诊断芯片对拉米夫定治疗慢性乙型肝炎过程中出现的肝炎病毒P基因区YMDD变异进行快速准确的检测方法。
To set up using the gene chip technology to detect and identify quickly and accurately the HBV P gene YMDD Motif mutation during the chronic hepatitis treated with lamivudine.
寻找新的可同时提高诊断方法的特异性和敏感性的基因重组抗原，是本研究尝试的目的之一。
Our purposes is disccussing if multivalence and multi-epitope gene recombination antigens can raise specificity and sensitivity simultaneously.
DNA杂交生物传感器为基因的识别及疾病的诊断提供了一种快速、简便、廉价的方法。
DNA molecular biosensor which based on the DNA hybridization offered a highly rapid and simple method for the detection of genetic variations and infectious disease pathogens.
因此，寻找恶性肿瘤的早期诊断指标以及寻找基因的靶向治疗方法逐渐成为一个研究的热点。
Therefore, seeking for indicators of early diagnosis of malignant tumors and to find targeted therapy of gene has gradually become a research direction.
方法1例经组织病理结合临床诊断为毛囊角化病，采用聚合酶链反应和DNA测序方法对此家系进行基因突变情况检测。
Methods A patient was diagnosed as Darier s disease by pathology and clinical features. PCR and DNA sequencing were used to detect the gene mutation of the family.
在基因组DNA水平，应用基因突变分析的方法对肾上腺脑白质营养不良进行分子诊断十分重要。
The molecular diagnosis for X linked adrenoleukodystrophy (ALD) using mutational analysis at genomic DNA level is important.
在基因组DNA水平，应用基因突变分析的方法对肾上腺脑白质营养不良进行分子诊断十分重要。
The molecular diagnosis for X linked adrenoleukodystrophy (ALD) using mutational analysis at genomic DNA level is important.
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