Deletion 16q Involving Partial 3’ Cbfbeta with an Additional Triple Trisomy; a Novel Finding in Aml M4 Eosinophilia; a Distinct Sub-Class-Reference-Cited by-同舟云学术

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Deletion 16q Involving Partial 3’ Cbfbeta with an Additional Triple Trisomy; a Novel Finding in Aml M4 Eosinophilia; a Distinct Sub-Class

Published:2024 Issue: Volume: Page:
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Author:

Abunaser suhaib,Pais Anurita,Ozturk Prof Cigdem Pala

Publisher

Elsevier BV

Reference16 articles.

1. Impact of cytogenetics on clinical outcome in AML;David Grimwade;Acute myelogenous leukemia,2007

2. Acute myeloid leukemia with recurrent genetic abnormalities;D A Arber;WHO Classification of Tumors of Hematopoietic and Lymphoid Tissues,2016

3. Acute myeloid leukemia with inv(16)(p13.1q22) and deletion of the 5'MYH11/3'CBFB gene fusion: a report of two cases and literature review;L Lv;Mol Cytogenet,2020

4. CBFB Break-Apart FISH Testing: An Analysis of 1629 AML Cases with a Focus on Atypical Findings and Their Implications in Clinical Diagnosis and Management;R K Yang;Cancers,2021

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