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The clinical application of array CGH for the detection of chromosomal defects in 20126 unselected newborns

机译：阵列CGH在20126例未选新生儿中检测染色体缺陷的临床应用

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摘要

BackgroundArray comparative genomic hybridization (CGH) is a powerful tool for detecting unbalanced chromosomal alterations. To validate the usefulness of array CGH in newborn screening, we examined 20,126 unselected infants. In addition, the number of newborns analyzed with array CGH is the largest one ever reported.

机译：BackgroundArray比较基因组杂交（CGH）是检测不平衡染色体改变的强大工具。为了验证阵列CGH在新生儿筛查中的有效性，我们检查了20126例未选择的婴儿。此外，使用阵列CGH分析的新生儿人数是有史以来最多的。

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期刊名称 Molecular Cytogenetics
作者
Sang-Jin Park; Eun Hye Jung; Ran-Suk Ryu; Hyun Woong Kang; He Doo Chung; Ho-Young Kang;
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作者单位

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年(卷),期 2013(6),-1
年度 2013
页码 21
总页数 5
原文格式 PDF
正文语种
中图分类遗传学;
关键词
Array CGH Newborns Chromosome abnormality;

机译：阵列CGH;新生儿;染色体异常;
入库时间 2022-08-17 11:42:33

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专利

1. The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns [J] . Sang-Jin Park, Eun Hye Jung, Ran-Suk Ryu, Molecular cytogenetics . 2013,第25期

机译：CGH阵列在20126例未选新生儿中检测染色体缺陷的临床应用
2. Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi Arabia [J] . Ibtessam Ramzi Hussein, Adeel G. Chaudhary, Randa Bassiouni, BMC Genomics . 2014,第2期

机译：阵列比较基因组杂交（阵列-CGH）在沙特阿拉伯发育延迟/先天性畸形患儿染色体失衡检测中的应用
3. Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies [J] . Lisa Edelmann, Kurt Hirschhorn Annals of the New York Academy of Sciences . 2008,第期

机译：阵列CGH检测与智力障碍和多发性先天性异常有关的染色体失衡的临床实用性
4. Detection of gene copy number change in array CGH data [C] . Jing Hu, Jianbo Gao, Yinhe Cao, IEEE/NLM Life Science Systems and Applications Workshop . 2006

机译：检测阵列CGH数据中基因拷贝数变化
5. Mosaicism for trisomy 21: Utility of array-based technology for its detection and its influence on telomere length and the frequency of acquired chromosome abnormalities. [D] . Charalsawadi, Chariyawan. 2011

机译：21三体马赛克：基于阵列技术的实用性，可用于检测其对端粒长度和获得性染色体异常的频率的影响。
6. Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi Arabia [O] . Ibtessam Ramzi Hussein, Adeel G Chaudhary, Randa Bassiouni, 2014

机译：阵列比较基因组杂交（array-CGH）在沙特阿拉伯发育延迟/先天性畸形患儿染色体失衡检测中的应用
7. The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns [O] . Sang-Jin Park, Eun Jung, Ran-Suk Ryu, 2013

机译：阵列CGH在20126例未选新生儿中检测染色体缺陷的临床应用
8. Detection of Genetic Alterations in Breast Sentinel Lymph Node by Array- CGH [R] . Cavalli, L. R. 2006

机译：阵列CGH检测乳腺前哨淋巴结遗传改变

The clinical application of array CGH for the detection of chromosomal defects in 20126 unselected newborns

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