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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.
Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, Ribeiro RC, de Jesus Marques-Salles T, Sobral ES, Gerardin Land MP, Liehr T. Macedo Silva ML, et al. Among authors: de jesus marques salles t, de figueiredo af. Cancer Genet Cytogenet. 2008 Apr 1;182(1):56-60. doi: 10.1016/j.cancergencyto.2007.12.014. Cancer Genet Cytogenet. 2008. PMID: 18328953
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21.
de Figueiredo AF, Mkrtchyan H, Liehr T, Soares Ventura EM, de Jesus Marques-Salles T, Santos N, Ribeiro RC, Abdelhay E, Macedo Silva ML. de Figueiredo AF, et al. Among authors: de jesus marques salles t. Cancer Genet Cytogenet. 2009 Sep;193(2):123-6. doi: 10.1016/j.cancergencyto.2009.05.001. Cancer Genet Cytogenet. 2009. PMID: 19665076
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 figueiredo af. Hematol Oncol. 2017 Dec;35(4):760-768. doi: 10.1002/hon.2299. Epub 2016 Jun 10. Hematol Oncol. 2017. PMID: 27282883
A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia.
de Jesus Marques-Salles T, Liehr T, Mkrtchyan H, Raimondi SC, Tavares de Souza M, de Figueiredo AF, Rouxinol S, Jordy Macedo FC, Abdelhay E, Santos N, Macedo Silva ML. de Jesus Marques-Salles T, et al. Among authors: de figueiredo af. Cancer Genet Cytogenet. 2009 Feb;189(1):59-62. doi: 10.1016/j.cancergencyto.2008.10.009. Cancer Genet Cytogenet. 2009. PMID: 19167614
A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosis.
de Souza DC, de Figueiredo AF, Mkrtchyan H, Othman MA, Liehr T, Dobbin J, Silva ML, Abdelhay E, Fernandez Tde S. de Souza DC, et al. Among authors: de figueiredo af. Blood Cells Mol Dis. 2014 Jun-Aug;53(1-2):91-3. doi: 10.1016/j.bcmd.2013.12.006. Epub 2014 Jan 14. Blood Cells Mol Dis. 2014. PMID: 24439112 No abstract available.
18 results