Browsing by Author Gil-da-Silva-Lopes, Vera Lucia

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Showing results 1 to 8 of 8
PreviewIssue DateTitleAuthor(s)AdvisorType
2006Cerebellar Involvement In Midline Facial Defects With Ocular Hypertelorism.Giffoni, Silvyo David Araújo; Gonçalves, Vanda Maria Gimenes; Zanardi, Verônica Araújo; Gil-da-Silva-Lopes, Vera Lucia-Artigo de periódico
2006Midline Facial Defects With Hypertelorism And Low-grade Astrocytoma: A Previously Undescribed Association.Giffoni, Silvyo David Araújo; Cendes, Fernando; Valente, Marcelo; Gil-da-Silva-Lopes, Vera Lucia-Artigo de periódico
2010Malformations of cortical development in patients with mid line facial defects and ocular hypertelorismAraujo Giffoni, Silvyo David; Cendes, Fernando; Valente, Marcelo; Gil-da-Silva-Lopes, Vera Lucia-Artigo
2012A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic stateFreitas, Erika L.; Gribble, Susan M.; Simioni, Milena; Vieira, Tarsis P.; Prigmore, Elena; Krepischi, Ana C.; Rosenberg, Carla; Pearson, Peter L.; Melo, Debora G.; Gil-da-Silva-Lopes, Vera Lucia-Artigo
2019Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public healthSgardioli, Ilaria Cristina; Monteiro, Fabiola Paoli; Fanti, Paulo; Vieira, Tarsis Paiva; Gil-da-Silva-Lopes, Vera Lucia-Artigo
2019Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergenceCruz, Pedro R. S.; Ananina, Galina; Gil-da-Silva-Lopes, Vera Lucia; Simioni, Milena; Menaa, Farid; Bezerra, Marcos A. C.; Domingos, Igor F.; Araujo, Aderson S.; Pellegrino, Renata; Hakonarson, Hakon; Costa, Fernando F.; Melo, Monica Barbosa de-Artigo
2019IRF6 polymorphisms in brazilian patients with non-syndromic cleft lip with or without palateBezerra, João Felipe; Silva, Heglayne Pereira Vital da; Bortolin, Raul Hernandes; Luchessi, André Ducati; Ururahy, Marcela Abbott Galvão; Loureiro, Melina Bezerra; Gil-da-Silva-Lopes, Vera Lucia; Almeida, Maria das Graças; Amaral, Viviane Souza do; Rezende, Adriana Augusto de-Artigo
2012Insertional translocation of 15q25‐q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridiaSimioni, Milena; Vieira, Tarsis Paiva; Sgardioli, Ilaria Cristina; Freitas, Erika Lopes; Rosenberg, Carla; Maurer-Morelli, Claudia Vianna; Lopes-Cendes, Iscia; Fett-Conte, Agnes Cristina; Gil-da-Silva-Lopes, Vera Lucia-Artigo
Showing results 1 to 8 of 8