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        Brazil's Craniofacial Project: Genetic Evaluation And Counseling In The Reference Network For Craniofacial Treatment. 

        Monlleó, Isabella Lopes; Gil-da-Silva-Lopes, Vera Lúcia (2006)

        Craniofacial and dental manifestations in Dubowitz syndrome - case report 

        Santos, Pedro Paulo de Andrade; Iglesias, Déborah Pitta Paraíso; Ribeiro, Betania Fachetti; Medeiros, Ana Miryam Costa de; Freitas, Roseana de Almeida; Souza, Lélia Batista de (2009)

        Craniofacial anomalies associated with hypospadias. Description of a hospital based population in South America 

        Fernandez, Nicolas; Escobar, Rebeca; Zarante, Ignacio (2016)
        Introduction: Hypospadias is a congenital abnormality of the penis, in which there is incomplete development of the distal urethra. There are numerous reports showing an increase of prevalence of hypospadias. Association ...

        Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient 

        CARVALHO, Daniel Rocha de; ROSSI, Natalia Freitas; SCHELLINI, Silvana; MORETTI-FERREIRA, Danilo; RICHIERI-COSTA, Antonio (WILEY-LISS, 2008)
        We report on a 4-year-old girl with blepharophimosis, a typical facial gestalt and skeletal abnormalities seen in the blepharofacioskeletal syndrome (BFSS). A comparative review with previous cases provides further evidence ...

        Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient 

        Universidade Estadual Paulista (Unesp); Universidade de São Paulo (USP) (Wiley-liss, 2008-08-15)
        We report on a 4-year-old girl with blepharophimosis, a typical facial gestalt and skeletal abnormalities seen in the blepharofacioskeletal syndrome (BFSS). A comparative review with previous cases provides further evidence ...

        Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient 

        Universidade Estadual Paulista (Unesp); Universidade de São Paulo (USP) (Wiley-liss, 2008-08-15)
        We report on a 4-year-old girl with blepharophimosis, a typical facial gestalt and skeletal abnormalities seen in the blepharofacioskeletal syndrome (BFSS). A comparative review with previous cases provides further evidence ...

        Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient 

        Carvalho, Daniel Rocha de; Rossi, Natalia Freitas; Schellini, Silvana Artioli; Moretti-Ferreira, Danilo; Richieri-Costa, Antonio (Wiley-liss, 2014)

        What Syndrome Is This? Oculocerebral Hypopigmentation Syndrome Of Preus. 

        de Oliveira Sobrinho, Ruy Pires; Steiner, Carlos Eduardo ()

        A cleft lip and palate gene, Irf6, is involved in osteoblast differentiation of craniofacial bone 

        University of Texas Health Science Center at Houston; Universidade Estadual Paulista (Unesp); University of Texas Health Science Center; University of Texas Health Science Center and MD Anderson Cancer Center at Houston (2019-03-01)
        Background: Interferon regulatory factor 6 (IRF6) plays a critical role in embryonic tissue development, including differentiation of epithelial cells. Besides orofacial clefting due to haploinsufficiency of IRF6, recent ...

        Fraser And Ablepharon Macrostomia Phenotypes: Concurrence In One Family And Association With Mutated Fras1. 

        Cavalcanti, Denise Pontes; Matejas, Verena; Luquetti, Daniela; Mello, Marcos Fernando; Zenker, Martin (2007)
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        Red de Repositorios Latinoamericanos
        + of 4.000.000
        Available publications
        163 Participating institutions
        Dirección de Servicios de Información y Bibliotecas (SISIB)
        Universidad de Chile
        Membership Login
        Featured collections
        • Latin American Theses
        • Argentinean Theses
        • Chilean Theses
        • Peruvian Theses
        Latest collections added
        • Argentina
        • Brazil
        • Colombia
        • México
        Dirección de Servicios de Información y Bibliotecas (SISIB)
        Universidad de Chile
        Red de Repositorios Latinoamericanos | 2006-2018