Search Results - "Garcia, Daniela R Ney"

Cell Cycle Kinetics and Sister Chromatid Exchange in Mosaic Turner Syndrome by Goulart, Miriam Beatriz, Vieira Neto, Eduardo, Garcia, Daniela R Ney, Guimarães, Marília Martins, de Paiva, Isaías Soares, de Ferran, Karina, Dos Santos, Nathalia Correia Krause, Barbosa, Luciana Santos, de Figueiredo, Amanda F, Ribeiro, Maria Cecília Menks, Ribeiro, Márcia Gonçalves

“…Turner syndrome (TS) is caused by a complete or partial absence of an X or Y chromosome, including chromosomal mosaicism, affecting 1 in 2500 female live…”
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A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome by de Souza, Daiane Correa, de Figueiredo, Amanda Faria, Ney Garcia, Daniela R, da Costa, Elaine Sobral, Othman, Moneeb A K, Liehr, Thomas, Abdelhay, Eliana, Silva, Maria Luiza Macedo, de Souza Fernandez, Teresa

“…Children with Down syndrome (DS) have an enhanced risk of developing acute leukemia, with the most common subtype being acute megakaryoblastic leukemia (AMKL)…”
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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 characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes by Ney Garcia, Daniela R., Souza, Mariana T., Figueiredo, Amanda F., Othman, Moneeb A. K., Rittscher, Katharina, Abdelhay, Eliana, Capela de Matos, Roberto R., Meyer, Claus, Marschalek, Rolf, Land, Marcelo G. P., Liehr, Thomas, Ribeiro, Raul C., Silva, Maria Luiza Macedo

“…In pediatric acute leukemias, reciprocal chromosomal translocations frequently cause gene fusions involving the lysine (K)‐specific methyltransferase 2A gene…”
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GAS6 Oncogene and Reverse MLLT3-KMT2A Duplications in an Infant with Acute Myeloid Leukemia and a Novel Complex Hyperdiploid Karyotype: Detailed High-Resolution Molecular Cytogenetic Studies by Capela de Matos, Roberto R, Ney Garcia, Daniela R, Cifoni, Elaine, Othman, Moneeb A K, Tavares de Souza, Mariana, Carboni, Edna K, Ferreira, Gerson M, Liehr, Thomas, Ribeiro, Raul C, M Silva, Maria Luiza

“…Pediatric acute myeloid leukemia (AML) is a highly heterogeneous disease, presenting cytogenetic and molecular abnormalities which turned out to be critical…”
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Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia by Ney-Garcia, Daniela R., Liehr, Thomas, Bhatt, Samarth, de Souza, Mariana T., Capela de Matos, Roberto R., Binato, Renata, Jordy, Fernanda C., Abdelhay, Eliana, Ribeiro, Raul C., Silva, Maria Luiza M.

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A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome by de Souza, Daiane Correa, de Figueiredo, Amanda Faria, Ney Garcia, Daniela R, da Costa, Elaine Sobral, Othman, Moneeb A K, Liehr, Thomas, Abdelhay, Eliana, Silva, Maria Luiza Macedo, de Souza Fernandez, Teresa

“…BACKGROUNDChildren with Down syndrome (DS) have an enhanced risk of developing acute leukemia, with the most common subtype being acute megakaryoblastic…”
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Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia by Ney-Garcia, Daniela R, Liehr, Thomas, Bhatt, Samarth, de Souza, Mariana T, de Matos, Roberto R Capela, Binato, Renata, Jordy, Fernanda C, Abdelhay, Eliana, Ribeiro, Raul C, Silva, Maria Luiza M

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