CranFlow: An Application for Record‐Taking and Management Through the Brazilian Database on Craniofacial Anomalies von Volpe‐Aquino, Roberta M., Monlleó, Isabella L., Lustosa‐Mendes, Elaine, Mora, Amanda F., Fett‐Conte, Agnes C., Félix, Têmis M., Xavier, Ana C., Tonocchi, Rita, Ribeiro, Erlane M., Pereira, Rui, Boy da Silva, Raquel T., Rezende, Adriana A., Cavalcanti, Denise P., Gil‐da‐Silva‐Lopes, Vera L.

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Identification of genomic imbalances in oral clefts von Lustosa-Mendes, Elaine, Santos, Ana P. dos, Vieira, Társis P., Ribeiro, Erlane M., Rezende, Adriana A., Fett-Conte, Agnes C., Cavalcanti, Denise P., Félix, Têmis M., Monlleó, Isabella L., Gil-da-Silva-Lopes, Vera Lúcia

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Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy von Moreira, Danielle P, Griesi-Oliveira, Karina, Bossolani-Martins, Ana L, Lourenço, Naila C V, Takahashi, Vanessa N O, da Rocha, Kátia M, Moreira, Eloisa S, Vadasz, Estevão, Meira, Joanna Goes Castro, Bertola, Debora, O'Halloran, Eoghan, Magalhães, Tiago R, Fett-Conte, Agnes C, Passos-Bueno, Maria Rita

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Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature von Monteiro, Fabíola P., Vieira, Társis P., Sgardioli, Ilária C., Molck, Miriam C., Damiano, Ana Paula, Souza, Josiane, Monlleó, Isabella L., Fontes, Marshall I. B., Fett-Conte, Agnes C., Félix, Têmis M., Leal, Gabriela F., M.Ribeiro, Erlane, Banzato, Claudio E. M., Dantas, Clarissa de R., Lopes-Cendes, Iscia, Gil-da-Silva-Lopes, Vera Lúcia

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A clinical study of 77 patients with mucopolysaccharidosis type II von Schwartz, Ida VD, Ribeiro, Márcia G, Mota, João G, Toralles, Maria Betânia P, Correia, Patrícia, Horovitz, Dafne, Santos, Emerson S, Monlleo, Isabella L, Fett-Conte, Agnes C, Sobrinho, Ruy P Oliveira, Norato, Denise YJ, Paula, Anna Carolina, Kim, Chong A, Duarte, Andréa R, Boy, Raquel, Valadares, Eugênia, De Michelena, Maria, Mabe, Paulina, Martinhago, Cyro D, Pina-Neto, João M, Kok, Fernando, Leistner-Segal, Sandra, Burin, Maira G, Giugliani, Roberto

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Influence of sleep disorders on the behavior of individuals with autism spectrum disorder von Fadini, Cintia C, Lamônica, Dionísia A, Fett-Conte, Agnes C, Osório, Elaine, Zuculo, Gabriela M, Giacheti, Célia M, Pinato, Luciana

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Clinical Features in Patients with 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities von Vieira, Társis P., Monteiro, Fabíola P., Sgardioli, Ilária C., Souza, Josiane, Fett-Conte, Agnes C., Monlleó, Isabella L., Fontes, Marshall B., Félix, Têmis, Leal, Gabriela F., Ribeiro, Erlane Marques, Gil-Da-Silva-Lopes, Vera L.

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Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) von Moreira, Eloisa S., Silva, Isabela M.W., Lourenço, Naila, Moreira, Danielle P., Ribeiro, Cintia M., Martins, Ana Luiza B., Griesi-Oliveira, Karina, Lazar, Monize, Costa, Silvia S., Naslavsky, Michel S., Rocha, Kátia M., Aguena, Meire, Fett-Conte, Agnes C., Zatz, Mayana, Rosenberg, Carla, Zachi, Elaine C., Bertola, Débora R., Vadasz, Estevão, Passos-Bueno, Maria Rita

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Feeding Infants with Cleft Lip and/or Palate in Brazil: Suggestions to Improve Health Policy and Research von Gil-Da-Silva-Lopes, Vera Lúcia, Xavier, Ana Carolina, Klein-Antunes, Denise, Ferreira, Ana Carolina R. G., Tonocchi, Rita, Fett-Conte, Agnes C., Silva, Raquel N., Leirião, Vera H. V., Caramori, Lázara P. C., Magna, Luiz A., Amstalden-Mendes, Lívia G.

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New complex chromosome abnormalities in multiple myeloma associated with a poor prognosis: A case report von Fett-Conte, Agnes C, Carvalho-Salles, Andréa B, Vendrame, Cristina B, Pedrassa, Patrícia, Freitas, Paula C, Varella-Garcia, Marileila

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Atypical chromosome abnormalities in acute myeloid leukemia type M4 von Fett-Conte, Agnes C., Estrela, Roseli Viscardi, Vendrame-Goloni, Cristina B., Carvalho-Salles, Andréa B., Ricci-Júnior, Octávio, Varella-Garcia, Marileila

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Time of diagnosis of oral clefts: a multicenter study von Amstalden-Mendes, Lívia G, Xavier, Ana Carolina, Antunes, Denise K, Ferreira, Ana Carolina R G, Tonocchi, Rita, Fett-Conte, Agnes C, Silva, Raquel N, Leirião, Vera H V, Caramori, Lázara P C, Magna, Luiz A, Gil-da-Silva-Lopes, Vera Lúcia

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Association between APOE polymorphisms and predisposition for autism von Giunco, Carina Tatiana, de Oliveira, Adriana B, Carvalho-Salles, Andréa B, Souza, Dorotéia S R, Silva, Ana Elizabete, da Rocha, Simone Secco, Fett-Conte, Agnes C

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Estudo multicêntrico da época do diagnóstico de fendas orais von Amstalden-Mendes, Lívia G, Xavier, Ana Carolina, Antunes, Denise K, Ferreira, Ana Carolina R. G, Tonocchi, Rita, Fett-Conte, Agnes C, Silva, Raquel N, Leirião, Vera H. V, Caramori, Lázara P. C, Magna, Luiz A, Gil-da-Silva-Lopes, Vera Lúcia

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Diagnóstico de hemoglobinopatias em recém-nascidos do Hospital de Base de São José do Rio Preto-SP von Siqueira, Fatima A. M., Fett-Conte, Agnes C., Borin, Leila N. B., Bonini-Domingos, Claudia R.

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A importância do gene p53 na carcinogênese humana von Fett-Conte, Agnes C., Salles, Andréa B. C. F.

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Investigação de hemoglobinopatias em sangue de cordão umbilical de recém-nascidos do Hospital de Base de São José do Rio Preto von Ducatti, Ricardo P., Teixeira, Antonio E.A., Galão, Heloísa A., Bonini-Domingos, Claudia R., Fett-Conte, Agnes C.

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Hemoglobina Köln diagnosticada em programa de triagem neonatal em São José do Rio Preto, SP von Schiaveto, Emanuele C., Vidotto, Alessandra, Siqueira, Fátima A.M., Naoum, Paulo C., Fett-Conte, Agnes C., Bonini-Domingos, Claudia R.

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New complex chromosome abnormalities in multiple myeloma associated with a poor prognosis: a case report von Fett-Conte, Agnes C, Carvalho-Salles, Andréa B, Vendrame, Cristina B, Pedrassa, Patrícia, Freitas, Paula C, Varella-Garcia, Marileila

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Leucemia mielóide crônica e o sistema Fas-FasL Chronic myeloid leukemia and the Fas-FasL system von Ana Paula F. Bergantini, Fabíola A. Castro, Ana M. Souza, Agnes C. Fett-Conte

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