Pariza PC, Stavarache I, Dumitru VA, et al. VACTERL association in a fetus with multiple congenital malformations – Case report. J Med Life. 2021 Nov-Dec;14(6):862-867. doi: 10.25122/jml-2021-0346.
Raam MS, Pineda-Alvarez DE, Hadley DW et al. Long-term outcomes of adults with features of VACTERL association. Eur J Med Genet. 2011 Jan-Feb;54(1):34-41. doi: 10.1016/j. ejmg.2010.09.007.
van de Putte R, de Walle HEK, van Hooijdonk KJM, et al. Maternal risk associated with the VACTERL association: A case- control study. Birth Defects Res. 2020 Nov;112(18):1495-1504. doi: 10.1002/bdr2.1773.
Jong E, Felix J, Deurloo J, et al. Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tra- cheoesophageal fistula and full or partial VACTERL association. Birth Defects Res 2008;82:92-7
La Placa S, Giuffrè M, Gangemi A et al. Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype? Ital J Pediatr. 2013 Jul 10;39:45. doi: 10.1186/1824-7288-39-45.