The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1.

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Published in Pediatr Nephrol on November 30, 2013

Authors

Anna Materna-Kiryluk1, Krzysztof Kiryluk, Katelyn E Burgess, Arkadiusz Bieleninik, Simone Sanna-Cherchi, Ali G Gharavi, Anna Latos-Bielenska

Author Affiliations

1: Department of Medical Genetics, Poznan University of Medical Sciences, Grunwaldzka 55/15, 60-352, Poznan, Poland, akiryluk@umed.poznan.pl.

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