1. Beckwith, J. B. (1963). Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas, and Leydig cell hyperplasia: Another syndrome? Abstract, Western society of Pediatric Research, Los Angeles.
2. Borer, J. G., Kaefer, M., Barnewolt, C. E., et al. (1999). Renal findings on radiological followup of patients with Beckwith-Wiedemann syndrome. Journal of Urology, 161, 235–239.
3. Brioude, F., Netchine, I., Praz, F., et al. (2015). Mutations of the imprinted CDKN1C gene as a cause of the overgrowth Beckwith-Wiedemann syndrome: Clinical spectrum and functional characterization. Human Mutation, 36, 894–902.
4. Eckmann-Scholz, C., & Jonat, W. (2011). 3-D ultrasound imaging of a prenatally diagnosed Beckwith-Wiedemann syndrome. Archives of Gynecology and Obstetrics, 284, 1051–1052.
5. Elliot, M., & Maher, E. R. (1994). Beckwith-Wiedemann syndrome. Journal of Medical Genetics, 31, 560–564.