Chromosome 22q11 Deletions in Patients with Conotruncal Heart Defects

@article{Khositseth2004Chromosome2D,
  title={Chromosome 22q11 Deletions in Patients with Conotruncal Heart Defects},
  author={Anant Khositseth and Chintana Tocharoentanaphol and Pongsak Khowsathit and Nichara Ruangdaraganon},
  journal={Pediatric Cardiology},
  year={2004},
  volume={26},
  pages={570-573}
}
We performed this study to determine the frequency of 22q11 deletions and associated phenotypic features and abnormalities in conotruncal heart defects. Sixty-one patients with conotruncal heart defects, including tetralogy of Fallot (TOF; n = 32), pulmonary atresia/ventricular septal defect (PAVSD; n = 12), double-outlet right ventricle (DORV; n = 5), transposition of the great arteries (TGA; n = 4 ), truncus arteriosus (TA; n = 4), subpulmonary ventricular septal defect (SPVSD; n = 3), and… CONTINUE READING

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