1Prader A, Labhart A, Willi H. Ein Syndrom von Adipositas, Kleinwuehs, Kryptorchismus und Oligophrenia nach myatonieartigem Zustand im Neugeborenenaher [ J]. Schweiz Med Wochenschr, 1956, 86: 1260-1261.
2McCandless SE; Committee on Genetics. Clinical report- health supervision for children with Prader-Willi syndrome [ J ]. Pediatrics, 2011, 127 ( 1 ) :195-204.
3Cassidy SB, Schwartz S, Miller JL, et al. Prader-Willi syndrome[J]. Genet Med, 2012, 14 (1): 10-26.
4Buffer MG. Pmder-Willi syndrome: obesity due to genomic imprinting [J]. Curr Genomics, 2011, 12 (3): 204-215.
5Goldstone AP, Holland AJ, Hauffa BP, et al. Recommendations for the diagnosis and management of Prader-Willi syndrome [ J]. J Clin Endocfinol Metab, 2008, 93 (11) : 4183-4197.
6Diene G, Mimoun E, Feigerlova E, et al. Endocrine dimmers in children with Pratter-Willi syndrome- data from 142 ehiidrert of the French database [J]. Horm Res Paediatr, 2010, 74 (2) : 121- 128.
7Emerick JE, Vogt KS. Endocrine manifestations and management of Prader-Willi syndrome [ J ]. Int J Pediatr Endocrinol, 2013, 2013 (1): 14.
8Lu W, Qi Y, Cui B, et al. Clinical and genetic features of Prader- Willi syndrome in China [ J]. Eur J Pediatr, 2014, 173 ( 1 ) : 81 - 86.
9Ma Y, Wu T, Liu Y, ct al. Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy [J]. J Pediatr Endocrinol Metal), 2012, 25 (11-12): 1103- 1109.
10Ehara H, Ohno K, Takeshita K. Frequency of the Prader-WiUi syndrome in the San-in district, Japan [J]. Brain Dev, 1995, 17 (5) : 324-326.