Surgical strategy for atrioventricular septal defect and tetralogy of Fallot or double-outlet right ventricle.
Raju V, Burkhart HM, Rigelman Hedberg N, Eidem BW, Li Z, Connolly H, Schaff HV, Dearani JA.
Ann Thorac Surg. 2013 Jun;95(6):2079-84; discussion 2084-5. doi: 10.1016/j.athoracsur.2013.02.016. Epub 2013 Apr 18.
Ten-year follow-up of dilatation of aortic structures in Fallot-type anomalies.
Kim W, Kwak JG, Cho S, Kim WH.
Pediatr Cardiol. 2023 Oct;44(7):1552-1559. doi: 10.1007/s00246-023-03225-7. Epub 2023 Jul 5.
Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle.
Tan ZP, Huang C, Xu ZB, Yang JF, Yang YF.
Clin Genet. 2012 Nov;82(5):466-71. doi: 10.1111/j.1399-0004.2011.01787.x. Epub 2011 Oct 30.
Pulmonary hypoplasia in fetuses with congenital conotruncal defects.
Wang Q, Zhao Y, Han L, Zhang Y, Ge S, He Y.
Echocardiography. 2017 Dec;34(12):1842-1851. doi: 10.1111/echo.13701.
Epidemiology of adult congenital heart disease among the general population in Kuwait.
Ashkanani H, Mohiyaldeen I, ElShenawy H, Alanbaei M.
Clin Cardiol. 2021 Apr;44(4):526-530. doi: 10.1002/clc.23569. Epub 2021 Feb 9.
Cyanotic congenital heart diseases among Nigerian children.
Animasahun BA, Madise-Wobo AD, Kusimo OY.
Cardiovasc Diagn Ther. 2017 Aug;7(4):389-396. doi: 10.21037/cdt.2017.06.03.
Correlating computed tomographic angiography of pulmonary circulation with clinical course and disease burden in patients with tetralogy of Fallot and pulmonary atresia.
Siripornpitak S, Kunjaru U, Sriprachyakul A, Promphan W, Katanyuwong P.
Eur J Radiol Open. 2021 Jun 15;8:100363. doi: 10.1016/j.ejro.2021.100363. eCollection 2021.
Anatomy of the ventricular septal defect in congenital heart defects: a random association?
Mostefa-Kara M, Houyel L, Bonnet D.
Orphanet J Rare Dis. 2018 Jul 18;13(1):118. doi: 10.1186/s13023-018-0861-z.
Prenatal diagnosis of fetal conotruncal defects by using 2D ultrasound and HD live flow combined with spatiotemporal image correlation.
Li TG, Su XR, Wu WR, Zhang WD, Ma B.
J Clin Ultrasound. 2023 Sep;51(7):1166-1171. doi: 10.1002/jcu.23454. Epub 2023 Mar 28.
Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
Park IS, Ko JK, Kim YH, Yoo HW, Seo EJ, Choi JY, Gil HY, Kim SJ.
Int J Cardiol. 2007 Jan 8;114(2):230-5. doi: 10.1016/j.ijcard.2005.12.029. Epub 2006 Jul 7.
