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:2013-11-30
Issue:2
Volume:29
Page:257-267
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ISSN:0931-041X
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Container-title:Pediatric Nephrology
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language:en
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Short-container-title:Pediatr Nephrol
Author:
Materna-Kiryluk Anna,Kiryluk Krzysztof,Burgess Katelyn E.,Bieleninik Arkadiusz,Sanna-Cherchi Simone,Gharavi Ali G.,Latos-Bielenska Anna
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology, and Child Health
Reference50 articles.
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