1)22q11DS22q11缺失综合征(22q11DS)
2)Chromosome 22q11 deletion syndrome22q11微缺失综合征
英文短句/例句
1.Study on Screening, Diagnosis and Intellectual Development Status in Children with Chromosome 22q11 Deletion Syndrome染色体22q11微缺失综合征的筛查与诊断及其智能发育状况的研究
2.Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation-dependent probe amplification多重连接探针扩增技术在先天性心脏病22q11微缺失/微重复综合征诊断中的应用
3.Study on the Relationship between 22q11 Microdeletion and Simple Congenital Heart Disease;单纯性先天性心脏病22q11微缺失的研究
4.Rapid Detection of the 22q11 Deletion with Quantitative Real-time PCR;实时荧光定量PCR快速诊断22q11微缺失
5.Detection of Y chromosome microdeletions in azoospermic patients with Klinefelter′s syndromeKlinefelter综合征Y染色体微缺失的检测
6.Analysis of the clinical phenotype and pathogenesis in seven children with 22q11.2 deletion syndrome.22q11.2微缺失综合征7例相关临床表型及病因分析
7.Establishment and Application of Genetic Diagnostic System for Eight Chromosome Microdeletion Syndromes by Fluorescence in Situ Hybridization;8种微缺失综合征荧光原位杂交诊断体系的建立与应用
8.Progresses on the genetic study of 22q11 deletion syndrome22号染色体长臂近端微片段缺失综合征的遗传学研究
9.acquired immunity deficiency syndrome获得性免疫缺乏综合征
10.sideropenic dysphagia syndrome缺铁性吞咽困难综合征
11.secondary antibody deficiency syndrome继发性抗体缺乏综合征
12.acquired immunodeficiency syndrome, AIDS获得性免疫缺陷综合征
13.Kallman syndrome性幼稚－失嗅综合征
14.Deletion of p15 Gene and Promoter Methylation in Myelodysplastic Syndromes骨髓增生异常综合征p15基因的表达缺失和启动子甲基化
15.Deletion of the p15 Gene and Promoter Methylation in the Bone Marrow of patients with Myelodysplastic Syndromes骨髓增生异常综合征患者骨髓p15基因的表达缺失与启动子甲基化
16.Establishment of RT-PCR for detection of nsp2 deletion porcine reproductive and respiratory syndrome virus猪繁殖与呼吸综合征病毒nsp2基因缺失株RT-PCR检测方法的建立
17.Muscle segment homeobox gene-1 and non-syndromic hypodontia同源异型盒基因-1与非综合征型多数牙先天性缺失
18.On College Student s Network Honest Lost and It s Comprehensive Treatment;浅谈大学生网络诚信缺失及综合治理
相关短句/例句
Chromosome 22q11 deletion syndrome22q11微缺失综合征
3)22q11.2 microdeletion syndrome染色体22q11·2微缺失综合征
1.Chromosome 22q11.染色体22q11·2微缺失综合征(22q11·2DS)是人类最常见的染色体微缺失综合征。
4)22q11 microdeletion22q11微缺失
1.Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases;先天性心脏病患者22q11微缺失检测及相关分析
2.Objective: The purpose of this study was to determine the frequency of 22q11 microdeletions in pediatric patients with simple congenital heart disease, the parental origin of the deleted chromosome, and relation of genotype to phenotypes.目的：检测单纯性先天性心脏病的患儿22q11微缺失的发生率及缺失来源与临床表型的关系，从遗传学角度探讨单纯性先天性心脏病发生的遗传学病因。
3.Reports showed that the major cardiac abnormality was conotruncal defects in patients with 22q11 microdeletion syndrome,while some patients with conotruncal defects had 22q11 microdeletion.研究证实,圆锥动脉干畸形是22q11微缺失综合征最常见的心脏表现,而部分圆锥动脉干畸形患者存在22q11微缺失。
5)deletion syndrome缺失综合征
1.Progresses on the genetic study of 22q11 deletion syndrome22号染色体长臂近端微片段缺失综合征的遗传学研究
6)5p deletion syndromes5p缺失综合征
1.The term "5p deletion syndromes" is proposed to encompass all the patients.通过对丹麦Niebuhr实验室所提供的106例5p缺失患者临床诊断资料和染色体分析资料的研究，首先定义了“5p缺失综合征”。
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。
