Genetic analysis of chromosome 22q11.2 markers in congenital heart disease

中國醫藥大學機構典藏 China Medical University Repository, Taiwan > 中醫學院 > 針灸研究所 > 期刊論文 > Item 310903500/5745

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.cmu.edu.tw/ir/handle/310903500/5745

题名:	Genetic analysis of chromosome 22q11.2 markers in congenital heart disease
作者:	施怡如(Shi YR);謝凱生(Hsieh KS);鄔哲源(Wu,Jer-Yuarn);李正淳(Lee,Chun-Cheng);蔡長海;余明宗(YU MT);張正成(Jeng-Sheng Chang);蔡輔仁(Fuu-Jen Tsai)*
贡献者:	中醫學院學士後中醫學系學士班中醫基礎學科;中國附醫基因醫學部
关键词:	CHD;STRP marker;chromosome 22q11.2;microdeletion
日期:	2003-05
上传时间:	2009-08-24 15:02:36 (UTC+8)
摘要:	Congenital heart disease (CHD) is a common cardiac defect found in infants and children. Despite advances in diagnosis and treatment, our understanding of the causative mechanism and etiology of CHD is limited. To determine the genetic etiology of CHD, we selected 11 consecutive short tandem-repeat polymorphic (STRP) markers located in the interval of the 22q11.2 region to perform genotype analysis on a large number of CHD patients (>120) and their normal relatives (>220). The results show that as regards the distribution of allelic size and frequency of these STRP markers, there were no significant differences between the CHD patients and the normal volunteers. This indicates that there is no linkage disequilibrium with these markers in CHD. In the level of heterozygosity for each marker in nonsyndromic CHD and conotruncal heart defect (CTD), there were no significant differences between the two populations. In syndromic CHD, the level of heterozygosity for D22S1648 was significantly lower than that observed in the unaffected population (2 = 11.25; P = 0.001). This suggests that there may be a deletion at the D22S1648 locus, and the low heterozygosity of D22S1648 indicates that this marker can be used as a genetic marker for detecting microdeletions in 22q11.2. With the use of fluorescence in situ hybridization (FISH) and real-time quantitative polymerase chain reaction (PCR) performed on syndromic patients, we confirmed the molecular results.
關聯:	JOURNAL OF CLINICAL LABORATORY ANALYSIS 17(1)28~35
显示于类别:	[針灸研究所] 期刊論文

文件中的档案:

档案	大小	格式	浏览次数
	0Kb	Unknown	479	检视/开启

在CMUR中所有的数据项都受到原著作权保护.

TAIR相关文章

数据加载中.....