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Browsing by Author Weber, Stefanie
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2006 | Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans | Schonfelder, EM; Knuppel, T; Tasic, Velibor; Miljkovic, Predrag; Konrad, Martin; Wuhl, E; Antignac, C; Bakkaloglu, A; Schaefer, F; Weber, Stefanie | Article | 21aM21a |
| 2024 | Phenotypic and genotypic spectrum of familial cases with congenital anomalies of the kidney and urinary tract (CAKUT) | Schniedermeier, Timo; Goldammer, Stephanie; Tasic, Velibor; Vollhardt, Anne; Abazi, Emini Nora; Gessner, Michaela; Putnik, Jovana; Stavileci, Valbona; Mueller, Dominik; Specht, Sabine;
Stajic, Natasa; Braunisch, Matthias C; Riedhammer, Korbinian Maria; Weber, Stefanie; Hoefele, Julia;
| Conference Paper | Mp. category will be shown later |
| 2006 | Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: Results of the ESCAPE study | Weber, Stefanie; Moriniere, Vincent; Knueppel, Tanja; Charbit, Marina; Dusek, Jiri; Ghiggeri, Gian Marco; Jankauskiene, Augustina; Mir, Sevgi; Montini, Giovanni; Peco-Antić, Amira  ;
Wuehl, Elke; Zurowska, Aleksandra M.; Mehls, Otto; Antignac, Corinne; Schaefer, Franz; Salomon, Remi;
| Article | 21a+M21a+ |