An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association

Authors

Benjamin D. Solomon, Inova Translational Medicine Institute
Linda A. Baker, UT Southwestern Medical Center
Kelly A. Bear, National Human Genome Research Institute (NHGRI)
Bridget K. Cunningham, National Human Genome Research Institute (NHGRI)
Philip F. Giampietro, University of Wisconsin-Madison
Colleen Hadigan, National Institute of Allergy and Infectious Diseases (NIAID)
Donald W. Hadley, National Human Genome Research Institute (NHGRI)
Steven Harrison, UT Southwestern Medical Center
Marc A. Levitt, Cincinnati Children's Hospital Medical Center
Nickie Niforatos, Childrens National Health System
Scott M. Paul, National Institutes of Health (NIH)
Cathleen Raggio, Hospital for Special Surgery - New York
Heiko Reutter, Universität Bonn
Nicole Warren-Mora, National Human Genome Research Institute (NHGRI)

Document Type

Journal Article

Publication Date

1-1-2014

Journal

Journal of Pediatrics

Volume

164

Issue

3

DOI

10.1016/j.jpeds.2013.10.086

APA Citation

Solomon, B., Baker, L., Bear, K., Cunningham, B., Giampietro, P., Hadigan, C., Hadley, D., Harrison, S., Levitt, M., Niforatos, N., Paul, S., Raggio, C., Reutter, H., & Warren-Mora, N. (2014). An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association. Journal of Pediatrics, 164 (3). http://dx.doi.org/10.1016/j.jpeds.2013.10.086