Scoliosis and rare diseases: our experience with the Prader–Willi syndrome
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00586-024-08247-0.pdf
Reference19 articles.
1. Fraccaro M, Zuffardi O, Buhler EM, Jurik LP (1977) 15/15 Translocation in Prader-Willi syndrome. J Med Genet 14(4):275–276. https://doi.org/10.1136/jmg.14.4.275
2. Cassidy SB, Driscoll DJ (2009) Prader-Willi syndrome. Eur J Hum Genet 17:3–13. https://doi.org/10.1038/ejhg.2008.165
3. Whittington JE, Holland AJ, Webb T, Butler J, Clarke D, Boer H (2001) Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region. J Med Genet 38:792–798. https://doi.org/10.1136/jmg.38.11.792
4. Smith A, Egan J, Ridley G, Haan E, Montgomery P, Williams K, Elliott E (2003) Birth prevalence of Prader-Willi syndrome in Australia. Arch Dis Child 88:263–264. https://doi.org/10.1136/adc.88.3.263
5. Butler MG, Thompson T (2000) Prader-Willi syndrome: clinical and genetic findings. Endocrinologist 10:3S-16S. https://doi.org/10.1097/00019616-200010041-00002
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