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American Journal of Medical Genetics. Part A|December 28, 2020
Cardiac evaluation of patients with 22q11.2 duplication syndromeAdam Butensky, Chiara Pandolfi de Rinaldis, Shrey Patel, et al.
American Heart Journal|September 11, 2013
Morbidity in children and adolescents after surgical correction of truncus arteriosus communisMichael L O'Byrne, Laura Mercer-Rosa, Huaqing Zhao, et al.
Pediatric Blood & Cancer|December 31, 2021
Late effects in survivors of high-risk neuroblastoma following stem cell transplant with and without total body irradiationWendy L Hobbie, Yimei Li, Claire Carlson, et al.
American Journal of Human Genetics|June 10, 2008
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephalyErich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, et al.
Pediatric Cardiology|September 17, 2013
Morbidity in children and adolescents after surgical correction of interrupted aortic archMichael L O'Byrne, Laura Mercer-Rosa, Huaqing Zhao, et al.
American Journal of Medical Genetics. Part A|March 9, 2005
The 22q11.2 deletion in African-American patients: an underdiagnosed population?Donna M McDonald-McGinn, Nancy Minugh-Purvis, Richard E Kirschner, et al.
Frontiers in Cardiovascular Medicine|August 9, 2021
Identifying Risk Factors for Complicated Post-operative Course in Tetralogy of Fallot Using a Machine Learning ApproachJennifer A Faerber, Jing Huang, Xuemei Zhang, et al.
Pediatric Cardiology|June 15, 2021
Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome Without Intracardiac AnomaliesChiara Pandolfi de Rinaldis, Adam Butensky, Shrey Patel, et al.
JTCVS Open|March 10, 2025
Surgical resection of diffuse pulmonary arteriovenous malformations (PAVMs)Aden R Falk, Lindsay J Nitsche, Colleen E Bontrager, et al.
Heart (British Cardiac Society)|June 29, 2014
Lean mass deficits, vitamin D status and exercise capacity in children and young adults after Fontan palliationCatherine M Avitabile, Mary B Leonard, Babette S Zemel, et al.
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