Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations
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PII: S1477-5131(06)00056-8
doi:10.1016/j.jpurol.2006.03.002
© 2006 Journal of Pediatric Urology Company. Published by Elsevier Inc. All rights reserved.
