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Updated: Jun 29, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

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全球发育迟缓和乌克兰儿童智力障碍的遗传决定因素

Khrystyna Shchubelka1,2, Liudmyla Turova3, Walter Wolfsberger1

  • 1Department of Biological Sciences, Oakland University, 118 Library Drive, Rochester, Yaroslava Hasynets, MI, 48309, USA.

Journal of neurodevelopmental disorders
|March 28, 2024
PubMed
概括

下一代测序 (NGS) 确定了乌克兰15.8%的儿科全球发育迟缓 (GDD) 和智力障碍 (ID) 病例的遗传原因. 这项研究强调了NGS基因面板和整个外体序列 (WES) 作为有价值的诊断工具,特别是在资源有限的环境中.

关键词:
基因组测试是基因组测试.全球发展的延迟.智力障碍 智力障碍是一种智力障碍.下一代测序测序是什么乌克兰. 乌克兰.整个外基因组的测序.

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