Search Results - "da Rocha, Moisés M"

Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8 by De Souza, Mariana T, Vera-Lozada, Gabriela, Othman, Moneeb, Marques-Salles, Teresinha J, Pinto, Luciana W, da Rocha, Moisés M, Rouxinol, Soraia, Liehr, Thomas, Ribeiro, Raul C, Hassan, Rocio, Silva, Maria Luiza M

“…Dear Editor, Burkitt lymphoma/leukemia (BL/L) was the first neoplasia associated with rearrangement in MYC that is the molecular hallmark of this disease…”
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An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia by Monteso, Kelly C.d.A., Othman, Moneeb A.K., Capela de Matos, Roberto R., Ney Garcia, Daniela R., da Rocha, Moisés M., de Souza, Mariana T., Albagli, Luiza F., Liehr, Thomas, Land, Marcelo G.P., Silva, Maria Luiza M., Costa, Elaine S.

“…KMT2A gene rearrangements represent the most frequent group of abnormalities in childhood leukemia (~70% of cases), with over 120 rearrangements described. The…”
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Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8 by De Souza, Mariana T, Vera-Lozada, Gabriela, Othman, Moneeb, Marques-Salles, Teresinha J, Pinto, Luciana W, da Rocha, Moisés M, Rouxinol, Soraia, Liehr, Thomas, Ribeiro, Raul C, Hassan, Rocio, Silva, Maria Luiza M

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