Amanda F. De Figueiredo
Rio De Janeiro, RJ 21941912, Brazil
Last Updated: 09/26/2026
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Found 10 publications
Cell Cycle Kinetics and Sister Chromatid Exchange in Mosaic Turner Syndrome.
Journal: Life (Basel, Switzerland)
Published: February 25, 2024
Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia.
Journal: British journal of haematology
Published: December 23, 2019
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
Journal: Hematological oncology
Published: October 15, 2015
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia.
Journal: Molecular cytogenetics
Published: June 25, 2015
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.
Journal: Acta haematologica
Published: March 16, 2015
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.
Journal: Blood cells, molecules & diseases
Published: September 06, 2013
Overexpression of the MLL gene combined with 11q trisomy in a child with acute lymphoblastic leukemia.
Journal: Clinical lymphoma, myeloma & leukemia
Published: July 16, 2013
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.
Journal: Blood cells, molecules & diseases
Published: September 04, 2012
A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).
Journal: Leukemia research
Published: October 27, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026