| 单词 | mutation analysis | ||||||||||||||||
| 释义 | mutation analysis
更多释义 收起释义 例句释义: 突变分析,变体分析,变异分析 1. Mutation analysis of the time coefficient shows that there was a pronounced weakening mutation of the zonal wind in 1967. 时间系数的突变分析表明纬向风在1967年发生了一次较明显的减弱突变； www.dqkxqk.ac.cn 2. Methods: Polymerase chain reaction(PCR), DNA direct nucleotide sequencing and RFLP were used in mutation analysis. 方法：PCR，DNA直接测序以及RFLP对患者的ECM1编码区进行了基因突变分析。 www.chemyq.com 3. HFE mutation analysis has strengthened our ability to diagnose HH accurately and is useful in family studies. HFE基因突变分析加强了我们的能力和准确诊断螺杆菌是有用的家庭研究。 www.syyxw.com 4. Genetic counseling and ANKRD26 mutation analysis should be offered to patients with autosomal-dominant thrombocytopenia. 而且，也应向常染色体显性血小板减少证患者提供遗传咨询和进行ANKRD26突变分析。 www.medlive.cn 5. This paper presents a technique for using mutation analysis to test the semantic correctness of XML-based component interactions. 本文提出一种变异分析技术来测试基于XML的网络异构组件交互的语义正确性。 www.ceps.com.tw 6. In ESTHER we use different tools to present the mutation analysis of cholinesterases and provide links to enzyme kinetics. 埃丝特我们在使用不同的工具目前，胆碱酯酶基因突变分析，并提供链接酶动力学研究。 goabroad.zhishi.sohu.com 7. Mutation analysis in families with XLHED allows for genetic counselling, prenatal diagnosis and gene therapy. 突变分析可以为今后XLHED的遗传咨询、产前诊断和基因治疗奠定基础。 www.fabiao.net 8. Gene mutation analysis was performed for patients with BH4 deficiency and their parents. 对BH4缺乏症者及父母进行基因突变检测。 d.wanfangdata.com.cn 9. Mutation Analysis for the Mitochondrial DNA in a Pedigree with Aminoglycoside Antibiotic Induced Deafness 一个氨基糖苷类抗生素致聋家系线粒体DNA突变研究 www.ilib.cn 10. Pathological features and gene mutation analysis in two pedigrees of diffuse palmoplantar keratoderma 两个弥漫性掌跖角化病家系的病理特征与基因突变分析 www.ilib.cn 1. Mutation Analysis of the IHH gene in two Chinese Families with Inherited Syndactyly and Adactylism 两个先天性并指缺指中国家系IHH基因的突变检测 www.ilib.cn 2. Mutation Analysis for Mitochondrial DNA in a Chinese Pedigree with Maternally Inherited Aminoglycoside Antibiotic-Induced Deafness 母系遗传氨基糖苷类抗生素致聋家系的线粒体DNA突变分析 www.ilib.cn 3. Gene mutation analysis of a Chinese family of congenital long QT syndromes 一中国先天性长QT综合征家系的基因突变分析 service.ilib.cn 4. Mutation analysis of a Chinese family with inherited long QT syndrome 先天性长QT综合征一家系的突变分析 service.ilib.cn 5. Mutation analysis of dystrophin gene and clinical evaluation of phenotypes in X-linked dilated cardiomyopathy X-连锁扩张型心肌病患者杜兴氏肌营养不良基因突变分析及临床评价 www.ilib.cn 6. Clinical, neuroimaging features and mutation analysis of genes in a large Chinese pedigree of chorea 舞蹈病家系临床、影像学特征及基因突变分析 service.ilib.cn 7. Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy 线粒体肌病患者线粒体DNA的突变分析 scholar.ilib.cn 8. Mutation analysis of genes associated with autosomal recessive in early-onset parkinsonism 常染色体隐性遗传早发性帕金森综合征致病基因的突变分析 www.ilib.cn 9. Mutation analysis of fibroblast growth factor receptor 3 gene in an achondroplasia family 一个软骨发育不全家系成纤维细胞生长因子受体3基因突变分析 www.ilib.cn 10. Advance in Mutation Analysis of the Candidate Genes in Premature Ovarian Failure 卵巢早衰候选基因的突变研究进展 www.ilib.cn 1. GNE gene mutation analysis in a family of distal myopathy with rimmed vacuoles 有镶边空泡远端肌病一家系GNE基因突变分析 www.ilib.cn 2. Mutation Analysis of Hematopoietic Cell Phosphatase Gene in Acute Leukemia 急性白血病细胞造血细胞磷酸酶基因的突变分析 www.ilib.cn 3. Mutation analysis of neurofilament-light gene in Chinese Charcot-Marie-Tooth disease 神经丝轻链基因在腓骨肌萎缩症中的突变分析 www.ilib.cn 4. Mutation analysis of androgen receptor gene in infertile men with oligospermia 少精不育患者的雄性激素受体基因突变分析 www.ilib.cn 5. The mutation analysis for HR and CDSN gene in a congenital alopecia family 一先天性秃发家系HR和CDSN基因突变的筛查 service.ilib.cn 6. The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7 脊髓小脑共济失调第7型的临床特征及基因突变研究 www.ilib.cn 7. Genetic linkage and mutation analysis of the candidate genes in a big family with autosomal dominant retinitis pigmentosa 常染色体显性视网膜色素变性家系的基因连锁定位和候选基因的序列分析 www.ilib.cn 8. Mutation analysis of tumor suppressor gene PTEN in bone and soft tissue tumors 肿瘤抑癌基因PTEN在骨及软组织肿瘤中的突变 www.ilib.cn 9. Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease 小热休克蛋白22基因在腓骨肌萎缩症中的突变分析 www.ilib.cn 10. Mouse Phenotypes: A Handbook Of Mutation Analysis 小鼠表型：突变分析手册 bibf.cnpbook.com 1. Mutation Analysis Based on Constructed Type Algebra Specification 基于构造类别代数的变异分析 www.ilib.cn 2. An Improved Method for Mutation Analysis 一种变异分析改进方法 service.ilib.cn 3. Mutation analysis of SHH gene in high myopia patients SHH基因在高度近视患者中的突变研究 www.ilib.cn 4. Mutation analysis of SHIP gene in acute leukemia 急性白血病细胞SHIP基因的突变分析 www.ilib.cn |
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