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Items : 3
Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature in American Journal of Medical Genetics, Part A
2009
ASL Vercelli
ASL Vercelli
Garavelli L; Zollino M; Cerruti Mainardi P; Gurrieri F; Rivieri F; Soli F; Verri R; Albertini E; Favaron E; Zignani M; Orteschi D; Bianchi P; Faravelli F; Forzano F; Seri M; Wischmeijer A; Turchetti D; Pompilii E; Gnoli M; Cocchi G; Mazzanti L; Bergamaschi R; De Brasi D; Sperandeo MP; Mari F; Uliana V; Mostardini R; Cecconi M; Grasso M; et alii...
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B): Report of three Italian cases with hypospadias and review in Hormone Research
2005
ASL Vercelli
ASL Vercelli
Garavelli L; Cerruti-Mainardi P; Virdis R; Pedori S; Pastore G; Godi M; Provera S; Rauch A; Zweier C; Zollino M; Banchini G; Longo N; Mowat D; Neri G; Bernasconi S;
Mowat-Wilson syndrome and mutation of the Zinc Finger Homeo Box 1B gene: A new syndrome probably under-diagnosed in Italian Journal of Pediatrics
2005
ASL Vercelli
ASL Vercelli
Cerruti Mainardi P; Garavelli L; Pastore G; Virdis R; Pedori S; Godi M; Provera S; Rauch A; Zweier C; Castronovo C; Zollino M; Banchini G; Bernasconi S; Neri G;