Search Results - Bruno Guimarães Marcarini
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Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum by Wilker Dias Martins, Elisa França Chaves, Flavia Cristina Gonçalves de Aquino, Sean Brasil de Oliveira, Isabela Dorneles Pasa, Bruno Guimarães Marcarini, Vitor Ribeiro Paes, Chong Ae Kim, Regina Schultz
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