5q脊髓性肌萎缩,5qSMA
1)5qSMA5q脊髓性肌萎缩
2)non-5qSMA非5q脊髓性肌萎缩
3)Spinal muscular atrophy脊髓性肌萎缩
1.Objective Spinal muscular atrophy (SMA) is one of common autosomal recessive diseases and is characterized by degeneration of the anterior horn cells of the spinal cord.目的脊髓性肌萎缩(spinal muscular atrophy,SMA)是以脊髓前角运动神经元退化变性为特征的一种常见的常染色体隐性遗传病。
2.Objective To establish a gene diagnosis assay for spinal muscular atrophy(SMA) in children.目的探讨儿童脊髓性肌萎缩症(SMA)的特异性基因诊断方法。
英文短句/例句

1.The Studies of the Detection and Expression of SMN Gene of Spinal Muscular Atrophy;脊髓性肌萎缩症SMN基因检测及其表达的研究
2.Gene Sequencing and Prenatal Diagnosis of Spinal Muscular Atrophy;脊髓性肌萎缩症基因测序及产前基因诊断
3.The Studies and Application of Gene Diagnosis for Spinal Muscular Atrophy;脊髓性肌萎缩症的基因诊断及其应用研究
4.Analysis of clinical manifestation and EMG in patients with spinal muscular atrophy accompanied by elevation of CK levels肌酸磷酸激酶增高的脊髓性肌萎缩症患者临床与肌电图分析
5.The Association Analysis between Spinal Muscular Atrophy 1 and Mitochondrial Genome;I型脊髓性肌萎缩症与线粒体基因组的相关性研究
6.Relationship between Expression of Zinc Finger Protein A20 mRNA and Apoptosis in Spinal Muscular Atrophy;锌指蛋白A20mRNA表达与脊髓性肌萎缩症细胞凋亡的关系
7.Study on the Gene Diagnosis and the Genotype-Phenotype Correlation of Spinal Muscular Atrophy;脊髓性肌萎缩症基因诊断及基因型与表型关系的研究
8.Establishment and Application of Haplotype Analysis and Single Cell PCR in Spinal Muscular Atrophy;脊髓性肌萎缩症单体型连锁分析和单细胞扩增方法的建立及应用研究
9.The Application of DHPLC in the Gene Diagnosis of the Childhood Type Spinal Muscular Atrophy and the Gene Screening of the SMA CarriersDHPLC技术在儿童型脊髓性肌萎缩症的基因诊断及携带者筛查中的应用
10.The Application of DHPLC in the Gene Diagnosis of the Childhood Type Spinal Muscular Atrophy and in the Gene Screening of the SMA CarriersDHPLC技术在儿童型脊髓性肌萎缩症的基因诊断及携带者基因筛查中的应用
11.progressive spinal muscular atrophy脊髓性进行性肌萎缩
12.syphilitic spinal muscular atroph梅毒性脊髓病性肌萎缩
13.hic muscular atrophy杜-阿二氏病;脊髓病性肌萎缩;脊髓性进行性肌萎缩
14.amyotrophic lateral sclerosisph.1. 肌萎缩性脊髓侧索硬化症
15.tabetic optic atrophy脊髓痨性视神经萎缩
16.How to confirm it is motor neuron amyotrophy resulting from spinal anterior horn cells damage如何判断脊髓灰质前角细胞病变引起的肌萎缩是运动神经元病性肌萎缩
17.Cycling Exercise、Fetal Tissue Transplants Restored the Muscle Atrophy after Spinal Cord Transaction in Rats;锻炼、胎体脊髓组织移植修复大鼠急性脊髓离断后肌肉萎缩的实验研究
18.Traumatic Spinal Cord Atrophy:A Case Report and Literature Review外伤性脊髓萎缩(1例报告及文献复习)
相关短句/例句

non-5qSMA非5q脊髓性肌萎缩
3)Spinal muscular atrophy脊髓性肌萎缩
1.Objective Spinal muscular atrophy (SMA) is one of common autosomal recessive diseases and is characterized by degeneration of the anterior horn cells of the spinal cord.目的脊髓性肌萎缩(spinal muscular atrophy,SMA)是以脊髓前角运动神经元退化变性为特征的一种常见的常染色体隐性遗传病。
2.Objective To establish a gene diagnosis assay for spinal muscular atrophy(SMA) in children.目的探讨儿童脊髓性肌萎缩症(SMA)的特异性基因诊断方法。
4)Spinal muscular atrophy脊髓性肌萎缩症
1.Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy;脊髓性肌萎缩症SMN1基因定量研究及基因携带者的筛查(英文)
2.Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography;应用变性高效液相色谱技术快速诊断儿童型脊髓性肌萎缩症(英文)
3.Prenatal diagnosis of spinal muscular atrophy based on umbilical cord blood;胎儿脐带血产前诊断脊髓性肌萎缩症
5)myelopathic muscular atrophy脊髓病性肌萎缩
6)progressive spinal muscular atrophy进行性脊髓性肌萎缩
延伸阅读

[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]分子式:C16H16ClN3O3S分子量:365.5CAS号:26807-65-8性质:暂无制备方法:暂无用途:用于轻、中度原发性高血压。