22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.

@article{MercerRosa201522q112DS,
  title={22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.},
  author={Laura Mercer-Rosa and Stephen M. Paridon and Mark A. Fogel and Jack Rychik and Ronn E. Tanel and Huaqing Zhao and Xuemei Zhang and Wei Yang and Justine Shults and Elizabeth Goldmuntz},
  journal={Circulation. Cardiovascular genetics},
  year={2015},
  volume={8 1},
  pages={74-81}
}
BACKGROUND Patients with repaired tetralogy of Fallot 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 patients with repaired tetralogy of Fallot. METHODS AND RESULTS We performed a cross-sectional study of tetralogy of Fallot subjects who were tested for 22q11.2 deletion, and underwent cardiac magnetic… CONTINUE READING
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