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An uncommon t(9;11)(p24;q22) with monoallelic loss of <italic>ATM</italic> and <italic>KMT2A</italic> genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.
- Published in:
- Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0389-x
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- Publication type:
- Article
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.
- Published in:
- Acta Haematologica, 2015, v. 134, n. 4, p. 243, doi. 10.1159/000431073
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- Article
Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia.
- Published in:
- British Journal of Haematology, 2020, v. 189, n. 6, p. e245, doi. 10.1111/bjh.16675
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- Article
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
- Published in:
- 2017
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- Publication type:
- journal article
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia.
- Published in:
- Cytogenetic & Genome Research, 2019, v. 157, n. 3, p. 213, doi. 10.1159/000499640
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- Publication type:
- Article
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.
- Published in:
- Cytogenetic & Genome Research, 2017, v. 152, n. 1, p. 33, doi. 10.1159/000477108
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- Publication type:
- Article