References
- Hamzeh G, Crespo A, Rey E, et al. Right aortic arch with aberrant left subclavian artery and anomalous origin of right pulmonary artery from ascending aorta. World J Pediatr Congenit Heart Surg 2011;2:324-6. https://doi.org/10.1177/2150135110389830
- Kanne JP, Godwin JD. Right aortic arch and its variants. J Cardiovasc Comput Tomogr 2010;4:293-300. https://doi.org/10.1016/j.jcct.2010.07.002
- Ryan AK, Goodship JA, Wilson DI, et al. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 1997;34:798-804. https://doi.org/10.1136/jmg.34.10.798
- Rubay JE, Sluysmans T, Alexandrescu V, et al. Surgical repair of coarctation of the aorta in infants under one year of age: long-term results in 146 patients comparing subclavian flap angioplasty and modified end-to-end anastomosis. J Cardiovasc Surg (Torino) 1992;33:216-22.
- Ito K, Kogure T, Hayashi S, et al. A case of the incomplete double aortic arch diagnosed in adulthood by MR imaging. Radiat Med 1995;13:263-7.
- Schlesinger AE, Krishnamurthy R, Sena LM, et al. Incomplete double aortic arch with atresia of the distal left arch: distinctive imaging appearance. AJR Am J Roentgenol 2005;184:1634-9. https://doi.org/10.2214/ajr.184.5.01841634