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Dive into the research topics of 'Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations'. Together they form a unique fingerprint.- Sort by
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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
Research output: Contribution to journal › Article › peer-review