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1.
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
Hematol Oncol
; 35(4): 760-768, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27282883
2.
Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents.
Pediatr Blood Cancer
; 61(8): 1422-6, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24668946
3.
A new chromosomal three-way rearrangement involving MLL masked by a t(9; 19)(p11; p13) in an infant with acute myeloid leukemia
Cancer Genet Cytogenet
; 189(1): 59-62, feb., 2009. ilus
Artículo
en Inglés
| TXTC | ID: txt-24366
4.
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
Cancer Genet Cytogenet
; 182(1): 56-60, apr., 2008. ilus
Artículo
en Inglés
| TXTC | ID: txt-24377
5.
A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1 : The Contribution of Molecular Approaches for Revealing t(8;21) Variants.
Acta Haematol
; 134(4): 243-5, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26138995
6.
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.
Blood Cells Mol Dis
; 53(1-2): 91-3, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24439112
7.
A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.
Blood Cells Mol Dis
; 50(2): 131-3, 2013 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-23044159
8.
BCR-ABL1 co-occurring with CBFA2T3-GLIS2 and RAM immunophenotype in a non-Down syndrome infant with acute megakaryoblastic leukemia.
Leuk Lymphoma
; 64(12): 2042-2046, 2023 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37548333
9.
An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.
Mol Cytogenet
; 11: 40, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30008805
10.
Chromosome 17 abnormalities and mutation of the TP53 gene: Correlationbetween cytogenetics, flow cytometry and molecular analysis in three casesof chronic myeloid leukemia
Genet. mol. biol
; 28(1): 40-43, 2005. ilus, graf
Artículo
en Inglés
| TXTC | ID: txt-25455
11.
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome.
Mol Cytogenet
; 10: 35, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28912835
12.
A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5.
Blood Cells Mol Dis
; 45(3): 197-8, 2010 Oct 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-20688548
13.
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia.
Mol Cytogenet
; 8: 62, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26257826
14.
High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia.
Mol Cytogenet
; 8: 45, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26136832
15.
Translocation (11;11)(p13- p15;q23) in a child with therapy-related acute myeloid leukemia following chemotherapy with DNA-topoisomerase II inhibitors for Langerhans cell histiocytosis.
Cancer Genet Cytogenet
; 135(1): 101-2, 2002 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-12072208
16.
Cytogenetic analysis of 100 consecutive newly diagnosed cases of acute lymphoblastic leukemia in Rio de Janeiro.
Cancer Genet Cytogenet
; 137(2): 85-90, 2002 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-12393277
17.
Cytogenetic analysis of 100 consecutive newly diagnosed cases of acutelymphoblastic leukemia in Rio de Janeiro
Cancer Genet Cytogenet
; 137(2): 85-90, 2002. ilus, graf
Artículo
en Inglés
| TXTC | ID: txt-24435
18.
Intrachromosomal amplification of chromosome 21 (iAMP21) detected by ETV6/RUNX1 FISH screening in childhood acute lymphoblastic leukemia: a case report.
Rev Bras Hematol Hemoter
; 35(5): 369-71, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24255623
19.
Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome.
Case Rep Genet
; 2012: 186532, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23074685
20.
Secondary acute myeloid leukemia with a t(1;11)(q23;p15) in an adolescent treated for testicular sarcoma.
Cancer Genet Cytogenet
; 169(1): 83-5, 2006 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-16875945