Found: 5
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A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome.
- Published in:
- Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0335-3
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- Publication type:
- 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
Cell Cycle Kinetics and Sister Chromatid Exchange in Mosaic Turner Syndrome.
- Published in:
- Life (2075-1729), 2024, v. 14, n. 7, p. 848, doi. 10.3390/life14070848
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- Publication type:
- 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