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Volume 39 Issue 4
Apr.  2012
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Article Contents

Prader–Willi Syndrome: 16-Year Experience in Hong Kong

doi: 10.1016/j.jgg.2012.02.005
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  • Corresponding author: E-mail address: luksite@gmail.com (Ho Ming Luk)
  • Received Date: 2011-12-29
  • Accepted Date: 2012-02-16
  • Rev Recd Date: 2012-02-15
  • Available Online: 2012-02-22
  • Publish Date: 2012-04-20
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    Mitchell, J., Schinzel, A., Langlois, S. et al. Comparison of phenotype in uniparental disomy and deletion Prader–Willi syndrome: sex specific differences Am. J. Med. Genet., 65 (1996),pp. 133-136
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    Sahoo, T., del Gaudio, D., German, J.R. et al. Prader–Willi phenotype caused by paternal deficiency for the HBIl-85 C/D box small nucleolar RNA cluster Nat. Genet., 40 (2008),pp. 719-721
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