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HNF1B nephropathy has a slow-progressive phenotype in childhood: with the exception of very early onset cases : results of the German Multicenter HNF1B Childhood Registry
by Okorn, Christine (Author)
, Tönshoff, Burkhard (Author)
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Pediatric nephrology, 34 (2019), 6, Seite 1065-1075
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Genomic profiling of papillary renal cell tumours identifies small regions of DNA alterations: a possible role of HNF1B in tumour development
by Szponar, Adrianna (Author)
, Yusenko, Maria V (Author)
, Kuiper, Roland (Author)
, van Kessel, Ad Geurts (Author)
, Kovacs, Gyula (Author)
,
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Histopathology, 58 (2011), 6, Seite 934-943
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Medizinische Fakultät Heidelberg
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Klinikum der Universität Heidelberg
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Zentrum für Kinder- und Jugendmedizin
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Kovacs, Gyula
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Kuiper, Roland
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Okorn, Christine
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Szponar, Adrianna
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Tönshoff, Burkhard
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Yusenko, Maria V
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van Kessel, Ad Geurts
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HNF1B
Cystic kidney disease
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GFR decline
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Hypomagnesemia
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MODY
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array-CGH
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immunohistochemistry
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papillary renal cell tumour
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precursor lesion
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