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1.
An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia.
J Pediatr Hematol Oncol
; 43(3): e371-e374, 2021 04 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32134839
2.
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.
Cytogenet Genome Res
; 157(4): 213-219, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30974445
3.
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.
Cytogenet Genome Res
; 152(1): 33-37, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28595195
4.
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
5.
Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia.
J Pediatr Hematol Oncol
; 39(2): e85-e91, 2017 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28212262
6.
Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia.
Br J Haematol
; 189(6): e245-e248, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32314797
7.
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
8.
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.
Cancer Genet
; 221: 25-30, 2018 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29405993
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