Browsing by Author Vieira, Társis Paiva

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Showing results 1 to 5 of 5
PreviewIssue DateTitleAuthor(s)AdvisorType
2015Distal 22q11.2 Microduplication Combined With Typical 22q11.2 Proximal Deletion: A Case Report.Molck, Miriam Coelho; Vieira, Társis Paiva; Simioni, Milena; Sgardioli, Ilária Cristina; dos Santos, Ana Paula; Xavier, Ana Carolina; Gil-da-Silva-Lopes, Vera Lúcia-Artigo de periódico
2012Insertional Translocation Of 15q25-q26 Into 11p13 And Duplication At 8p23.1 Characterized By High Resolution Arrays In A Boy With Congenital Malformations And Aniridia.Simioni, Milena; Vieira, Társis Paiva; Sgardioli, Ilária Cristina; Freitas, Erika Lopes; Rosenberg, Carla; Maurer-Morelli, Cláudia Vianna; Lopes-Cendes, Iscia; Fett-Conte, Agnes Cristina; Gil-da-Silva-Lopes, Vera Lúcia-Artigo de periódico
2013Atypical Copy Number Abnormalities In 22q11.2 Region: Report Of Three Cases.Molck, Miriam Coelho; Vieira, Társis Paiva; Sgardioli, Ilária Cristina; Simioni, Milena; Dos Santos, Ana Paula; Souza, Josiane; Monteiro, Fabíola Paoli; Gil-da-Silva-Lopes, Vera Lúcia-Artigo de periódico
2013Partial Monosomy 21 (q11.2→q21.3) Combined With 3p25.3→pter Monosomy Due To An Unbalanced Translocation In A Patient Presenting Dysmorphic Features And Developmental Delay.dos Santos, Ana Paula; Vieira, Társis Paiva; Simioni, Milena; Monteiro, Fabíola Paoli; Gil-da-Silva-Lopes, Vera Lúcia-Artigo de periódico
2020Brazil's craniofacial project : different approaches on orofacial clefts and 22q11.2 deletion syndromeGil-da-Silva-Lopes, Vera Lúcia; Tacla, Milena Atique; Sgardioli, Ilária Cristina; Vieira, Társis Paiva; Monlleó, Isabella Lopes-Artigo