Omphalocele
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-07524-7_78
Reference12 articles.
1. Carli D, Bertola C, Cardaropoli S, et al. Prenatal features in Beckwith-Wiedemann syndrome and indications for prenatal testing. J Med Genet. 2021;58:842–9.
2. Corey KM, Hornik CP, Laughon MM, et al. Frequency of anomalies and hospital outcomes in infants with gastroschisis and omphalocele. Early Hum Dev. 2014;90(8):421–4.
3. Danzer E, Victoria T, Bebbington MW, et al. Fetal MRI-calculated total lung volumes in the prediction of short-term outcome in giant omphalocele: preliminary findings. Fetal Diagn Ther. 2012;31(4):248–53.
4. Danzer E, Gerdes M, D’Agostino JA, et al. Patient characteristics are important determinants of neurodevelopmental outcome during infancy in giant omphalocele. Early Hum Dev. 2021;591(3):187–93.
5. Danzer E, Hoffman C, Miller JS, et al. Autism spectrum disorder and neurodevelopmental delays in children with giant omphalocele. J Pediatr Surg. 2019;54(9):1771–7.
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