FORZANO, Serena

FORZANO, Serena  

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Titolo Data di pubblicazione Autore(i) File
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient 2010 Ferrero GB; Howald C; Micale L; Biamino E; Augello B; Fusco C; Turturo MG; Forzano S; Reymond A; Merla G.
An atypical 7q11.23 deletion in a normal IQ Williams-Beurensyndrome patient 2009 Biamino E; Howald C; Micale L; Augello B; Fusco C; Turturo MG; Forzano S; Silengo M; Ferrero GB ; Reymond A; Merla G
Clinical manifestations in a cohort of 32 children with 22q11 deletion syndrome 2007 Delmonaco A.G; Ferrero G.B; Belligni E; Biamino E; Asnaghi V; Banaudi E; Martino S; Verdun Di Cantogno L; Forzano S; Cirillo Silengo M.
Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients 2007 FERRERO G; BIAMINO E; SORASIO L; BANAUDI E; PERUZZI L; FORZANO S; VERDUN DICANTOGNO L; SILENGO MC
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis. 2010 Lalatta F; Quagliarini D; Folliero E; Cavallari U; Gentilin B; Castorina P; Forzano F; Forzano S; Grosso E; Viassolo V; Naretto VG; Gattone S; Ceriani F; Faravelli F; Gargantini L.