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1.
Mechanism of Riverbed Aggradation at Tongguan Reach and Channel Shrinkage at Lower Weihe River;
潼关高程抬升与渭河淤积萎缩成因分析
2.
Cause Analysis of Shrinkage and Protection Countermeasure of Huihe Wetland in Hulunbeier City
呼伦贝尔辉河湿地萎缩成因分析及保护对策
3.
Cause of Shrinkage of Some Small Towns in Zhejiang and the Road to Development;
浙江部分小城镇萎缩的成因与发展对策
4.
Genetic Polymorphism in HOGG1 and Susceptibility to Chronic Atrophic Gastritis, Gastric Cancer;
HOGG1在萎缩性胃炎及胃癌中基因多态性分析
5.
Pathogenesis Reseach And Clinical Study Of Amyotrophic Lateral Sclerosis;
肌萎缩侧索硬化临床病例分析及病因研究
6.
Application of DNA sequence analysis in the research of distribution of cytokine gene polymorphisms in patients with chronic atrophic gastritis
DNA序列分析对慢性萎缩性胃炎细胞因子基因多态性分布的研究
7.
limbs withered by disease and starvation
因疾病和饥饿而造成的四肢萎缩.
8.
The Collection of Ancient Literature about Atrophy Diseases and a Research on 50 Cases of Amyotrophic Lateral Sclerosis Symptoms and Syndromes;
古代痿证病因病机文献整理及50例肌萎缩侧索硬化症证分析
9.
Black Pepper s Reducing in Planting Area in Lujiang Flatland and Its Development;
潞江坝胡椒种植面积严重萎缩原因分析及发展建议
10.
Polymorphisms in GSTT1, GSTM1 and CYP1A1 Genes and Risk of Sporadic Amyotrophic Lateral Sclerosis
散发性肌萎缩侧索硬化患者GSTT1、M1,CYP1A1基因多态性分析
11.
A Preliminary Study of Voxel-based Analysis in the Brain of Patients with Amyotrophic Lateral Sclerosis by Using MRI
肌萎缩侧索硬化症基于体素分析的脑部磁共振成像初步研究
12.
partial paralysis resulted in an atrophied left arm.
因为萎缩的左手而部分瘫痪。
13.
Fitting artificial eye on the atrophied eye of the teenager and children.
少年儿童眼球萎缩的义眼装配分析
14.
.NULL.;
我国农业保险业务萎缩的经济学分析
15.
A retrospective analysis of 58 cases of atrophic cholecystitis treated by laparoscopic cholecystectomy
腹腔镜治疗萎缩性胆囊炎58例分析
16.
The Early Diagnosis and Clinical Analysis of 19 Cases of Multiple System Atrophy
19例多系统萎缩临床分析及早期诊断
17.
Cause for the Decrease of Adult Students at Present and Countermeasures
当前成人高等教育生源萎缩的原因及应对策略
18.
Gene Mapping, Mutation Analysis of Neurofilament-light Gene and Study of Brainstem Auditory Evoked Potentials in Chinese Charcot-Marie-Tooth Disease Patients;
腓骨肌萎缩症的疾病基因定位、NEFL基因突变分析及脑干听觉诱发电位研究