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Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia.
Silva ML, Pombo-de-Oliveira MS, Raimondi SC, Mkrtchyan H, Abdelhay E, de Figueiredo AF, de Souza MT, Garcia DR, de Ventura EM, de Sousa AM, Liehr T. Silva ML, et al. Among authors: de sousa am, de souza mt, de figueiredo af, de ventura em. Mol Cytogenet. 2009 Feb 19;2:7. doi: 10.1186/1755-8166-2-7. Mol Cytogenet. 2009. PMID: 19228396 Free PMC article.
An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia.
Monteso KCDA, Othman MAK, Capela de Matos RR, Ney Garcia DR, da Rocha MM, de Souza MT, Albagli LF, Liehr T, Land MGP, Silva MLM, Costa ES. Monteso KCDA, et al. Among authors: de souza mt. J Pediatr Hematol Oncol. 2021 Apr 1;43(3):e371-e374. doi: 10.1097/MPH.0000000000001776. J Pediatr Hematol Oncol. 2021. PMID: 32134839
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.
Capela de Matos RR, Othman M, Ferreira GM, Monteso K, de Souza MT, Rouxinol M, Melo JB, Carreira IM, Abdelhay E, Liehr T, Ribeiro RC, Silva M. Capela de Matos RR, et al. Among authors: de souza mt. Cancer Genet. 2022 Apr;262-263:16-22. doi: 10.1016/j.cancergen.2021.12.003. Epub 2021 Dec 22. Cancer Genet. 2022. PMID: 34974289
Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia.
Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, de Matos RR, Binato R, Jordy FC, Abdelhay E, Ribeiro RC, Silva ML. Ney-Garcia DR, et al. Among authors: de souza mt, de matos rr. Leuk Lymphoma. 2012 Feb;53(2):342-4. doi: 10.3109/10428194.2011.613134. Epub 2011 Sep 29. Leuk Lymphoma. 2012. PMID: 21848362 No abstract available.
Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis.
de Souza MT, Mkrtchyan H, Hassan R, Ney-Garcia DR, de Azevedo AMB, da Costa ES, de Figueiredo AF, Liehr T, Abdelhay E, Silva MLM. de Souza MT, et al. Among authors: de figueiredo af, de azevedo amb. Int J Hematol. 2011 Feb;93(2):232-236. doi: 10.1007/s12185-010-0757-8. Epub 2011 Jan 5. Int J Hematol. 2011. PMID: 21207210
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
Ney Garcia DR, de Souza MT, de Figueiredo AF, Othman MAK, Rittscher K, Abdelhay E, Capela de Matos RR, Meyer C, Marschalek R, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Ney Garcia DR, et al. Among authors: de souza mt, de figueiredo af. Hematol Oncol. 2017 Dec;35(4):760-768. doi: 10.1002/hon.2299. Epub 2016 Jun 10. Hematol Oncol. 2017. PMID: 27282883
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.
Capela de Matos RR, Othman MAK, Ferreira GM, Costa ES, Melo JB, Carreira IM, de Souza MT, Lopes BA, Emerenciano M, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Capela de Matos RR, et al. Among authors: de souza mt. Cancer Genet. 2018 Feb;221:25-30. doi: 10.1016/j.cancergen.2017.12.002. Epub 2017 Dec 19. Cancer Genet. 2018. PMID: 29405993 Free article.
51 results