Novel CDH3 variants in Brazilian families with hypotrichosis and juvenile macular dystrophy revealed by exome sequencing von Schauren, Juliana S., Torres, Ana C.M.B.G., Almeida, Rodrigo C., Santos, Pablo S.C., Mulinari‐Brenner, Fabiane, Lima, Luiz H., Zago Filho, Luiz A., Shiokawa, Naoye, Bicalho, Maria da Graça, Sato, Mario T.

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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil von Krepischi, Ana C. V., Villela, Darine, da Costa, Silvia Souza, Mazzonetto, Patricia C., Schauren, Juliana, Migliavacca, Michele P., Milanezi, Fernanda, Santos, Juliana G., Guida, Gustavo, Guarischi-Sousa, Rodrigo, Campana, Gustavo, Kok, Fernando, Schlesinger, David, Kitajima, Joao Paulo, Campagnari, Francine, Bertola, Debora R., Vianna-Morgante, Angela M., Pearson, Peter L., Rosenberg, Carla

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CCR5 promoter region polymorphisms in systemic lupus erythematosus von Schauren, Juliana da Silveira, Oliveira, Amanda Henrique, Consiglio, Camila Rosat, Monticielo, Odirlei André, Xavier, Ricardo Machado, Nunes, Natália Schneider, Ellwanger, Joel Henrique, Chies, José Artur Bogo

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SIRT1 promoter polymorphisms as clinical modifiers on systemic lupus erythematosus von Consiglio, Camila Rosat, Juliana da Silveira, Schauren, Monticielo, Odirlei André, Xavier, Ricardo Machado, Brenol, João Carlos Tavares, Chies, José Artur Bogo

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