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Updated: Jun 8, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

注意欠陥多動性障害における希少な染色体欠損および重複:全ゲノム分析

Nigel M Williams1, Irina Zaharieva, Andrew Martin

  • 1MRC Centre in Neuropsychiatric Genetics and Genomics and Department of Psychological Medicine and Neurology, Cardiff University School of Medicine, Cardiff, UK. williamsnm@cf.ac.uk

Lancet (London, England)
|October 5, 2010
PubMed
まとめ

コピーナンバー変種 (CNVs) は,注意欠陥多動性障害 (ADHD) で有意に増加し,ADHDが単なる社会的構造ではないという遺伝的証拠を提供します. この研究は,ADHDの発達における遺伝因子の役割を強調しています.

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Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations08:22

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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