This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Abbott ME, Dawson WT. The clinical classification of congenital cardiac disease, with remarks upon its pathological anatomy, diagnosis and treatment. International Clinics 1924; 4: 156–88.AbbottMEDawsonWTThe clinical classification of congenital cardiac disease, with remarks upon its pathological anatomy, diagnosis and treatmentInternational Clinics1924415688Search in Google Scholar
Oppenheimer-Dekker A, Bartelings MM, Wenink ACG. Anomalous architecture of the ventricles in hearts with overriding of aortic valve and a perimembranous ventricular septal defect (“Eisenmenger VSD”) International Journal of Cardiology 1989; 9(3): 341–55.Oppenheimer-DekkerABartelingsMMWeninkACGAnomalous architecture of the ventricles in hearts with overriding of aortic valve and a perimembranous ventricular septal defect (“Eisenmenger VSD”)International Journal of Cardiology1989933415510.1016/0167-5273(85)90032-4Search in Google Scholar
Anderson RH, Weinberg PM. The clinical anatomy of tetralogy of fallot. Cardiol Young 2005; Suppl1: 38-47.15934690AndersonRHWeinbergPMThe clinical anatomy of tetralogy of fallotCardiol Young2005384710.1017/S1047951105001010Search in Google Scholar
Bailliard F, Anderson RH. Tetralogy of Fallot. Orphanet J Rare Dis 2009.19144126BailliardFAndersonRHTetralogy of FallotOrphanet J Rare Dis200910.1186/1750-1172-4-2Search in Google Scholar
McCord MC, Van Elk J, Blount SG Jr. Tetralogy of Fallot; clinical and hemodynamic spectrum of combined pulmonary stenosis and ventricular septal defect. Circulation 1957; 16(5): 736-49.1347304610.1161/01.CIR.16.5.736McCordMCVan ElkJBlountSG JrTetralogy of Fallot; clinical and hemodynamic spectrum of combined pulmonary stenosis and ventricular septal defectCirculation195716573649Search in Google Scholar
Shinebourne EA, Babu Narayan SV, Carvalho JS. Tetralogy of Fallot: from fetus to adult. Heart 2006; 92(9): 1353-59.1690872310.1136/hrt.2005.061143ShinebourneEABabu NarayanSVCarvalhoJSTetralogy of Fallot: from fetus to adultHeart2006929135359Search in Google Scholar
Apitz C, Webb GD, Redington AN. Tetralogy of Fallot. Lancet 2009; 374(9699): 1462-71.10.1016/S0140-6736(09)60657-719683809ApitzCWebbGDRedingtonANTetralogy of FallotLancet20093749699146271Open DOISearch in Google Scholar
Roessler E, Ouspenskaia MV, Karkera JD, Vélez JI, Kantipong A, Lacbawan F, Bowers P, Belmont JW, Towbin JA, Goldmuntz E, Feldman B, Muenke M. Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly. Am J Hum Genet 2008; 83(1): 18-29.10.1016/j.ajhg.2008.05.01218538293RoesslerEOuspenskaiaMVKarkeraJDVélezJIKantipongALacbawanFBowersPBelmontJWTowbinJAGoldmuntzEFeldmanBMuenkeMReduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephalyAm J Hum Genet20088311829244385418538293Open DOISearch in Google Scholar
Huang RT, Wang J, Xue S, Qiu XB, Shi HY, Li RG, Qu XK, Yang XX, Liu H, Li N, Li YJ, Xu YJ, Yang YQ. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. Int J Med Sci 2017; 14(4): 323-32.10.7150/ijms.1783428553164HuangRTWangJXueSQiuXBShiHYLiRGQuXKYangXXLiuHLiNLiYJXuYJYangYQTBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosusInt J Med Sci201714432332543647428553164Open DOISearch in Google Scholar
Qian Y, Xiao D, Guo X, Chen H, Hao L, Ma X, Huang G, Ma D, Wang H. Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation. J Transl Med 2017; 15(1): 69.10.1186/s12967-017-1173-028372585QianYXiaoDGuoXChenHHaoLMaXHuangGMaDWangHMultiple gene variations contributed to congenital heart disease via GATA family transcriptional regulationJ Transl Med201715169537952028372585Open DOISearch in Google Scholar
Lu CX, Gong HR, Liu XY, Wang J, Zhao CM, Huang RT, Xue S, Yang YQ. A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot. Int J Mol Med 2016; 37(2): 445-51.2667610510.3892/ijmm.2015.2436LuCXGongHRLiuXYWangJZhaoCMHuangRTXueSYangYQA novel HAND2 loss-of-function mutation responsible for tetralogy of FallotInt J Mol Med20163724455126676105Search in Google Scholar
Chen B, Gagnon M, Shahangian S, Anderson NL, Howerton DA, Boone JD; Centers for Disease Control and Prevention (CDC). Good Laboratory Practices for Molecular Genetic Testing for Heritable Diseases and Conditions. MMWR Recomm Rep 2009; 58(RR-6): 1-37.19521335ChenBGagnonMShahangianSAndersonNLHowertonDABooneJDCenters for Disease Control and Prevention (CDC). Good Laboratory Practices for Molecular Genetic Testing for Heritable Diseases and ConditionsMMWR Recomm Rep200958RR-6137Search in Google Scholar
