Isochromosome 7p, i(7)(p10): A rare AML, myelodysplasia-related entity
We describe genomic findings in an AML case with isochromosome 7p, i(7)(p10), in which SNP array analysis uncovered an additional 7.07-Mb 20q deletion not detected by karyotyping. Several AML cases with i(7)(p10) as an isolated cytogenetic finding have been previously reported. Based on consequent l...
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| Asıl Yazarlar: | , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2023-01-01
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| Seri Bilgileri: | Leukemia Research Reports |
| Konular: | |
| Online Erişim: | http://www.sciencedirect.com/science/article/pii/S2213048923000274 |
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