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Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|November 19, 2011
A case of bullous pemphigoid in infancy treated with local corticosteroidsL Atzori, M Pau, R Podda, et al.
Human Mutation|January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37D Gasperini, L Perseu, P Cossu, et al.
International Journal of Dentistry|October 24, 2012
Er:YAG Laser and Fractured Incisor Restorations: An In Vitro StudyC Fornaini, S Petruzzella, R Podda, et al.
Human Molecular Genetics|September 1, 1994
Mutations in the vasopressin V2-receptor gene in three families of Italian descent with nephrogenic diabetes insipidusV Faà, M L Ventruto, S Loche, et al.
The Journal of Pediatrics|August 1, 1995
A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydrationG B Leoni, S Pitzalis, R Podda, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|November 19, 2011
A case of bullous pemphigoid in infancy treated with local corticosteroidsL Atzori, M Pau, R Podda, et al.
Human Mutation|January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37D Gasperini, L Perseu, P Cossu, et al.
International Journal of Dentistry|October 24, 2012
Er:YAG Laser and Fractured Incisor Restorations: An In Vitro StudyC Fornaini, S Petruzzella, R Podda, et al.
Human Molecular Genetics|September 1, 1994
Mutations in the vasopressin V2-receptor gene in three families of Italian descent with nephrogenic diabetes insipidusV Faà, M L Ventruto, S Loche, et al.
The Journal of Pediatrics|August 1, 1995
A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydrationG B Leoni, S Pitzalis, R Podda, et al.
Pageof 1