Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
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Clin J Am Soc Nephrol. 2013 Jul;8(7):1179-87. doi: 10.2215/CJN.10221012. Epub 2013 Mar 28.
Clin J Am Soc Nephrol. 2013.
PMID: 23539225
Free PMC article.