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Mostrati risultati da 1 a 5 di 5
Clinical manifestations in a cohort of 32 children with 22q11 deletion syndrome
2007-01-01 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
2007-01-01 FERRERO G; BIAMINO E; SORASIO L; BANAUDI E; PERUZZI L; FORZANO S; VERDUN DICANTOGNO L; SILENGO MC
An atypical 7q11.23 deletion in a normal IQ Williams-Beurensyndrome patient
2009-01-01 Biamino E; Howald C; Micale L; Augello B; Fusco C; Turturo MG; Forzano S; Silengo M; Ferrero GB ; Reymond A; Merla G
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient
2010-01-01 Ferrero GB; Howald C; Micale L; Biamino E; Augello B; Fusco C; Turturo MG; Forzano S; Reymond A; Merla G.
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.
2010-01-01 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.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| 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 | |
| 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. | |
| 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. |
Mostrati risultati da 1 a 5 di 5
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