Osteogenesis imperfecta in Brazilian patients von Trancozo, Maira, Moraes, Marcos V D, Silva, Dalila A, Soares, Jéssica A M, Barbirato, Clara, Almeida, Márcio G, Santos, Lígia R, Rebouças, Maria R G O, Akel, Jr, Akel N, Sipolatti, Valentim, Nunes, Vanda R R, Errera, Flavia I V, Aguena, Meire, Passos-Bueno, Maria R, Paula, Flavia de

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Analysis of 12 X-STRs loci in a population from southeastern Brazil von Garcia, Fernanda M, Trabach, Raquel S R, Stange, Victor S, Cancian, Bruno, Zetum, Alexia S S, Casotti, Matheus C, Errera, Flavia I V, de Carvalho, Elizeu F, Meira, Débora D, Louro, Iuri D

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Functional Vascular Endothelial Growth Factor -634G>C SNP Is Associated With Proliferative Diabetic Retinopathy: A case-control study in a Brazilian population of European ancestry von Errera, Flavia I.V, Canani, Luís Henrique, Silva, Maria Elisabeth R, Yeh, Erika, Takahashi, Walter, Santos, Katia G, Souto, Katia E.P, Tschiedel, Balduíno, Roisenberg, Israel, Gross, Jorge Luis, Passos-Bueno, Maria Rita

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COL18A1 is highly expressed during human adipocyte differentiation and the SNP c.1136C > T in its "frizzled" motif is associated with obesity in diabetes type 2 patients von Errera, Flavia I V, Canani, Luís H, Yeh, Erika, Kague, Erika, Armelin-Corrêa, Lucia M, Suzuki, Oscar T, Tschiedel, Balduíno, Silva, Maria Elizabeth R, Sertié, Andréa L, Passos-Bueno, Maria Rita

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Functional vascular endothelial growth factor -634GC SNP is associated with proliferative diabetic retinopathy: a case-control study in a Brazilian population of European ancestry von Errera, Flavia I.V, Canani, Luis Henrique, Silva, Maria Elisabeth R, Yeh, Erika, Takahashi, Walter, Santos, Katia G, Souto, Katia E.P, Tschiedel, Balduino, Roisenberg, Israel, Gross, Jorge Luis, Passos-Bueno, Maria Rita

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Mutations in collagen 18A1 and their relevance to the human phenotype von Passos-Bueno, Maria Rita, Suzuki, Oscar T, Armelin-Correa, Lucia M, Sertié, Andréa L, Errera, Flavia I V, Bagatini, Kelly, Kok, Fernando, Leite, Katia R M

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Osteogenesis imperfecta in Brazilian patients von Trancozo, Maira, Moraes, Marcos V.D., Silva, Dalila A., Jéssica A.M. Soares, Barbirato, Clara, Almeida, Márcio G., Santos, Lígia R., Rebouças, Maria R. G. O., Akel N. Akel Jr, Sipolatti, Valentim, Nunes, Vanda R. R., Errera, Flavia I. V., Meire Aguena, Passos-Bueno, Maria R., Paula, Flavia De

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Mutations in Collagen 18A1 (COL18A1) and theirrelevance to the human phenotype von Lucia M. Armelin-Correa, Flavia I. V. Errera, Kelly Bagatini, Fernando Kok, Katia R. M. Leite, Maria Rita Passos-Bueno, Oscar T. Suzuki, André L. Sertié

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Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology? von Faria, Ágatha Cristhina, Rabbi-Bortolini, Eliete, Rebouças, Maria R. G. O., de S. Thiago Pereira, Andréia L. A., Frasson, Milena G. Tonini, Atique, Rodrigo, Lourenço, Naila Cristina V., Rosenberg, Carla, Kobayashi, Gerson S., Passos-Bueno, Maria Rita, Errera, Flávia Imbroisi Valle

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