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TrialPediatric nephrology (Berlin, Germany)2024

Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.

Marcin Kołbuc et al.PubMed ↗Full text ↗Publisher ↗

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4 papers cite it

2024
2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 38196016