Trisomy 8 is the Most Frequent Cytogenetic Abnormality in de novo Myelodysplastic Syndrome in China
Author:
Publisher
S. Karger AG
Subject
Cancer Research,Oncology,Hematology,General Medicine
Reference31 articles.
1. Myelodysplasia
2. Cross-validation of prognostic scores in myelodysplastic syndromes on 386 patients from a single institution confirms importance of cytogenetics
3. Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes
4. Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes
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1. Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality;Hematology;2022-05-12
2. Clinical significance of cytogenetic and molecular genetic abnormalities in 634 Chinese patients with myelodysplastic syndromes;Cancer Medicine;2021-02-20
3. Cytogenetic characteristics of 665 patients with myelodysplastic syndrome in China: A single‑center report;Oncology Letters;2020-12-17
4. Efficacy, safety and pharmacokinetics of subcutaneous azacitidine in Chinese patients with higher risk myelodysplastic syndromes: Results from a multicenter, single-arm, open-label phase 2 study;Asia-Pacific Journal of Clinical Oncology;2017-12-28
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