Rare copy number variants in patients with congenital conotruncal heart defects

Author:

Xie Hongbo M.1,Werner Petra2,Stambolian Dwight3,Bailey-Wilson Joan E.4,Hakonarson Hakon5,White Peter S.6,Taylor Deanne M.1,Goldmuntz Elizabeth2

Affiliation:

1. The Department of Biomedical and Health Informatics; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

2. Division of Cardiology; Children's Hospital of Philadelphia; Philadelphia Pennsylvania

3. Department of Ophthalmology and Human Genetics; School of Medicine, University of Pennsylvania; Philadelphia Pennsylvania

4. Statistical Genetics Section; National Human Genome Research Institute, National Institutes of Health; Baltimore Maryland

5. The Center for Applied Genomics; Department of Pediatrics, The Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania; Philadelphia Pennsylvania

6. Division of Biomedical Informatics; Cincinnati Children's Hospital, Department of Biomedical Informatics, University of Cincinnati; Cincinnati Ohio

Funder

National Institutes of Health

National Center for Research Resources

National Center for Advancing Translational Sciences

National Eye Institute

Pennsylvania Department of Health

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

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