22q11微重复,22q11 duplication英语短句,例句大全

22q11微重复,22q11 duplication
1)22q11 duplication22q11微重复
1.Results MLPA demonstrated that 7 cases had 22q11 deletion [6 cases from CLTCL1 to LZTR1( LCR A-D) and 1 case from CLTCL1 to PCQAP ( LCR A-C) ]and that 1 case had 22q11 duplication,spanning from ZNF74 to LZTR1( LCR B-D).结果195例患儿中,共检出22q11微缺失者7例(LCRA-D区6例,LCRA-C区1例),22q11微重复1例(LCRB-D区),涉及的CHD类型包括室间隔缺损、房室间隔缺损、肺动脉狭窄和法洛四联征。
2)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。

英文短句/例句

1.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
2.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
3.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
4.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
5.Research on 22q11.2 Microdeletion in Patients with Cono-truncal Deformanity;心脏圆锥动脉干畸形22q11.2微缺失的研究
6.The relationship of the down-expression/deletion of miR-15a and diseases微RNA miR-15a的下调/缺失与疾病的关系
7.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
8.The Divine Order of Things and the Order of Man:A Study of the Absence of Subjectivity in Traditional Chinese Ethics天道与人道——传统道德主体性缺失探微
9.the mote in a person's eye他人眼睛里的微尘; 他人的小缺点 [小过失]
10.The Absence of Gratitude of Hobbledehoy and Research on the School s Education Method;青少年感恩缺失与学校感恩教育策略探微
11.The Pathological Studying on the Testi-Cular Biopsy of Azoospermia of Azoospermia Factor Microdeletions;AZF基因微缺失无精子症患者睾丸病理观察
12.Talking about the Shortcomings and Countermeasures of Modern Chinese Literature Microcosmic Practice Teaching;中国现当代文学微观实践教学的缺失及其对策
13.On Deficiencies of the Traditional Faulty Wording Analysis in Contemporary Pragmatic Context;当代语用背景下传统语病分析之缺失探微
14.Maximum Likelihood Estimates for Missing Data of Micro Econometric Analysis;微观计量分析中缺失数据的极大似然估计
15.Analysis of Failure of Perventricular Device Closure of Ventricular Septal Defect微创外科室间隔缺损封堵失败原因分析
16.Chromosomal and Y chromosome microdeletion analysis in patients with oligozoospermia男性少精子患者染色体和Y染色体微缺失检查
17.Study on the correlation between the loss of microsatellite heterozygosity and thyroid carcinoma微卫星杂合性缺失与甲状腺癌相关性研究
18.Screening of the microdeletion in the Y chromosome azoopspermia factor region in 178 cases of male infertility178例男性不育患者Y染色体AZF微缺失筛查

相关短句/例句

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。
3)Chromosome 22q11 deletion syndrome22q11微缺失综合征
4)Micro-duplication微重复
5)Microsatellite repeats微卫星重复
6)Microsatellite repeats微随体重复