Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations

  • Dagan Jenkins
  • , Maria Bitner-Glindzicz
  • , Louise Thomasson
  • , Sue Malcolm
  • , Stephanie A. Warne
  • , Sally A. Feather
  • , Sarah E. Flanagan
  • , Sian Ellard
  • , Coralie Bingham
  • , Lane Santos
  • , Mark Henkemeyer
  • , Andrew Zinn
  • , Linda A. Baker
  • , Duncan T. Wilcox
  • , Adrian S. Woolf

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