Case report: CD8 positive T-cell Prolymphocytic Leukemia presenting complex karyotype with a rare chromosomal abnormality der(2)t(1;2)(q21;q37) and additional signals of the genes MYC, IGH, and TP53
Saved in:
| Main Authors: | Valderez Ravaglio Jamur, Mateus de Oliveira Lisboa, Ana Paula Azambuja, Paulo Roberto Slud Brofman |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-12-01
|
| Series: | Hematology, Transfusion and Cell Therapy |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2531137923001645 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Two ways to complex karyotype in MDS—the role of del(5q) and TP53
by: Sandra Huber, et al.
Published: (2025-05-01) -
Emergence of IGH::CCND1 rearrangement and mutations in TP53, BTK, and BCL2 associated with therapy resistance in chronic lymphocytic leukemia
by: Qing Wei, et al.
Published: (2024-12-01) -
Myc dynamically and preferentially relocates to a transcription factory occupied by Igh.
by: Cameron S Osborne, et al.
Published: (2007-08-01) -
Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13
by: Javier Sánchez, et al.
Published: (2014-01-01) -
P107: Co-existing t(9;14)(q33;q32)/IGH rearrangement is a risk factor for lymphoid blast phase transformation of chronic myeloid leukemia
by: Arash Ronaghy, et al.
Published: (2025-01-01)