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Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2014
Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesionsPeter S White, Hongbo M Xie, Petra Werner, et al.
Cardiology in the Young|July 8, 2016
Adult CHD: the ongoing need for physician counselling about heredity and contraceptive optionsCamila Londono-Obregon, Elizabeth Goldmuntz, Brooke T Davey, et al.
Human Mutation|September 9, 2014
Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart diseasePetra Werner, Prasuna Paluru, Anisha M Simpson, et al.
The Journal of Pediatrics|July 24, 2017
Exercise Performance and 22q11.2 Deletion Status Affect Quality of Life in Tetralogy of FallotElizabeth Goldmuntz, Amy Cassedy, Laura Mercer-Rosa, et al.
HGG Advances|March 29, 2022
Maternal effect genes as risk factors for congenital heart defectsFadi I Musfee, Omobola O Oluwafemi, A J Agopian, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 2, 2018
Right Ventricular Contractile Reserve Is Impaired in Children and Adolescents With Repaired Tetralogy of Fallot: An Exercise Strain Imaging StudyShivani M Bhatt, Yan Wang, Okan U Elci, et al.
Pediatric Cardiology|August 20, 2018
Determinants of Exercise Performance in Children and Adolescents with Repaired Tetralogy of Fallot Using Stress EchocardiographyShivani M Bhatt, Okan U Elci, Yan Wang, et al.
Plos One|May 8, 2014
Genome-wide association study of maternal and inherited loci for conotruncal heart defectsA J Agopian, Laura E Mitchell, Joseph Glessner, et al.
Pediatrics|December 5, 2003
Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomaliesDoff B McElhinney, Deborah A Driscoll, Elissa R Levin, et al.
BMC Medical Genetics|May 14, 2005
Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA)Nadja Muncke, Beate Niesler, Ralph Roeth, et al.
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