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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:Circ Cardiovasc Genet
Hoofdauteurs: Mercer-Rosa, Laura, Paridon, Stephen M., Fogel, Mark A., Rychik, Jack, Tanel, Ronn E., Zhao, Huaqing, Zhang, Xuemei, Yang, Wei, Shults, Justine, Goldmuntz, Elizabeth
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2015
Onderwerpen:
Article
Online toegang: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
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items