1. ASHG/ACMG Test and Technology Transfer Committee. (1996). Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee. American Journal of Human Genetics, 58, 1085–1088.
2. Aughton, D. J., & Cassidy, S. B. (1990). Physical features of Prader-Willi syndrome in neonates. American Journal of Diseases of Children, 144, 1251–1254.
3. Bieth, E., Eddiry, S., Gaston, V., et al. (2015). Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome. European Journal of Human Genetics, 23, 252–255.
4. Bray, G., Dahms, W., Swerdloff, R., et al. (1983). The Prader-Willi syndrome: A study of 40 patients and a review of the literature. Medicine, 62, 59–80.
5. Buiting, K. (2010). Prader-Willi syndrome and Angelman syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 154C, 365–376.