Sfoglia per AUTORE
CERRUTI-MAINARDI P
Collezione ASL Vercelli
Items : 3
Infantile cortical hyperostosis and COL1A1 mutation in four generations. in European journal of pediatrics / Eur J Pediatr. 2011 Nov;170(11):1385-90. doi: 10.1007/s00431-011-1463-0. Epub 2011 May 13.
2011
ASL Vercelli
ASL Vercelli
Cerruti-Mainardi P; Venturi G; Spunton M; Favaron E; Zignani M; Provera S; Dallapiccola B;
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;
Epidemiological investigation on the incidence of malignant tumours in children in the Vercelli province during the years 1975-1979 in Minerva Pediatrica
1985
ASL Vercelli
ASL Vercelli
Cerruti-Mainardi P; Colombino G; Colombo R;