ロード中...

22q11.2 Deletion Status and Disease Burden in Children and Adolescents with Tetralogy of Fallot

BACKGROUND: Patients with repaired tetralogy of Fallot (TOF) experience variable outcomes for reasons that are incompletely understood. We hypothesize that genetic variants contribute to this variability. We sought to investigate the association of 22q11.2 deletion status with clinical outcome in pa...

詳細記述

保存先:
書誌詳細
出版年:Circ Cardiovasc Genet
主要な著者: Mercer-Rosa, Laura, Paridon, Stephen M., Fogel, Mark A., Rychik, Jack, Tanel, Ronn E., Zhao, Huaqing, Zhang, Xuemei, Yang, Wei, Shults, Justine, Goldmuntz, Elizabeth
フォーマット: Artigo
言語:Inglês
出版事項: 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4383312/
https://ncbi.nlm.nih.gov/pubmed/25561045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.114.000819
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!