Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case–control study followed by systematic review of existing evidence
Version of Record online: 25 FEB 2011
© 2011 The Author(s)/Acta Pædiatrica © 2011 Foundation Acta Pædiatrica
Volume 100, Issue 7, pages 966–971, July 2011
How to Cite
Long, J., Zhang, S., Fang, X., Luo, Y. and Liu, J. (2011), Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case–control study followed by systematic review of existing evidence. Acta Paediatrica, 100: 966–971. doi: 10.1111/j.1651-2227.2011.02176.x
- Issue online: 2 JUN 2011
- Version of Record online: 25 FEB 2011
- Accepted manuscript online: 27 JAN 2011 01:53PM EST
- Received 13 November 2010; revised 12 January 2011; accepted 19 January 2011.
Vol. 101, Issue 11, 1184, Version of Record online: 1 OCT 2012
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