Genotype and phenotype in patients with Prader–Willi Syndrome in Taiwan
Version of Record online: 24 MAY 2007
©2007 The Author(s)/Journal Compilation © 2007 Foundation Acta Pædiatrica/Acta Pædiatrica
Volume 96, Issue 6, pages 902–905, June 2007
How to Cite
Lin, H.-Y., Lin, S.-P., Chuang, C.-K., Chen, M.-R., Yen, J.-L., Lee, Y.-J., Huang, C.-Y., Tsai, L.-P., Niu, D.-M., Chao, M.-C. and Kuo, P.-L. (2007), Genotype and phenotype in patients with Prader–Willi Syndrome in Taiwan. Acta Paediatrica, 96: 902–905. doi: 10.1111/j.1651-2227.2007.00284.x
- Issue online: 24 MAY 2007
- Version of Record online: 24 MAY 2007
- Received 14 October 2006; revised 22 January 2007; accepted 19 February 2007.
The following supplementary material is available for this article:
Table S1. Percentage of patients with Prader-Willi syndrome exhibiting characteristic features in two series
Table S2. Incidence of various features of Prader-Willi syndrome among patients with deletion or UPD
Table S3. Comparison of clinical manifestations in Prader-Willi syndrome caused by deletion versus UPD
Table S4. Comparison from different countries of proportions of Prader-Willi syndrome caused by deletion versus UPD
This material is available as part of the online article from: http://www.blackwell-synergy.com/doi/abs/10.1111/j.1651-2227.2007.00284.x (This link will take you to the article abstract).
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