DRD的例句大全

Conclusion The mutation rate of TH gene in Chinese patients with AR-DRD is low, hence suggesting the genetic heterogeneity and a new locus for AR-DRD.

结论TH基因在中国人AR-DRD家系中突变率不高，提示我国AR-DRD患者具有遗传异质性，可能存在新的致病基因。

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objective to study the clinical characteristics of patients with dopa-responsive dystonia ( drd).

目的研究多巴反应性肌张力障碍患者的临床特点。

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Conclusion: The results are uncertain whether the DRD 2、 DRD 3、 DRD 4、 DAT 1、 COMT 、5-HTR _ 2 A 、5-HTT gene are associated with obsessive compulsive spectrum disorders.

结论: 未能验证DRD2、DRD3、DRD4、DAT1、COMT、 5-HTR2A、5-HTT基因与OCSDs的 连锁关系,但亦不能排除这些基因与OCSDs的相关性.

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Conclusions Clinical diversity and diurnal fluctuation are the characteristics of DRD.

结论　DRD患者具有症状多样及日间波动的特点.

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Objective To summarize the clinical characteristics of dopa-responsive dystonia ( DRD ).

目的　总结多巴反应性肌张力不全 ( DRD ) 的临床特征.

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Objective To study the clinical characteristics of patients with dopa-responsive dystonia ( DRD ).

目的研究多巴反应性 肌 张力障碍患者的临床特点.

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Objective To investigate the clinical characteristics and GCHgene mutations in patients with dopa-responsive dystonia ( DRD ).

目的探讨多巴反应性肌张力障碍 ( DRD ) 临床及GTP环 化水解酶(GCH)基因突变特点.

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Objective To explore the pathogeny, clinical characteristics and therapy of dopa-responsive dystonia ( DRD ).

目的探讨多巴反应性肌张力障碍 ( DRD ) 的病因 、 临床特点及治疗,加强对该病的认识.

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Objective To explore the clinical feature and treatment method of the dopa-responsive dystonia ( DRD ).

目的探讨多巴反应性 肌 张力障碍的临床特点及治疗.

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Objective To explore the clinical feature and treatment method of the dopa responsive dystonia ( DRD ).

目的　探讨多巴反应性 肌 张力障碍的临床特点及治疗.

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Objective To analyze the clinical characteristics of dopa-responsive dystonia ( DRD ).

目的　分析对多巴反应性肌张力障碍 ( DRD ) 的临床特点.

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Objective The clinical features, diagnostic and therapeutic methods in dopa-responsive dystonia ( DRD ) were studied.

目的探讨多巴反应性 肌 张力障碍的临床特点 、 诊断和治疗方法.

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Objectives To investigate the DRD 2 genetic susceptibility to essential tremor ( ET ) in Chinese.

目的　探讨多巴胺D2受体基因多态与ET 遗传 易患者.

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Conclusion : The polymorphism of DRD 2 gene at TaqI site may have no effect on TD.

结论　DRD2基因TaqI多态性可能与TD的发生无关联性.

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Objective: to explore the relation of a marker ( TaqIA ) located DRD 2 gene and heroin dependence.

目的: 探讨多巴胺 ( DA ) 受体D2亚型基因TaqIA多态性与海洛因依赖者行为之间的相关性.

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Conclusion The clinical manifestations of DRD are various and they are closely correlated with age.

结论多巴反应性肌张力障碍临床表现呈多样化,临床表现与年龄密切相关.

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CONCLUSION: GCH 1 gene mutation is only one of reasons to the DRD patients onset.

结论: GCH-1 基因突变只是部分DRD患者的发病原因.

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Objective : To investigate the clinical characteristics and mutations of GCH I gene of patients with DRD.

目的: 研究DRD患者的临床特点和GCH基因突变.

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