Supplementary Table 2 from Somatic Exonic Deletions in <i>RUNX1</i> Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
<p>Supplementary Table 2</p>
محفوظ في:
| المؤلف الرئيسي: | Anna Eriksson (15352461) (author) |
|---|---|
| مؤلفون آخرون: | Marie Engvall (9184887) (author), Lucy Mathot (15352464) (author), Albin Österroos (15352467) (author), Martin Rippin (15352470) (author), Lucia Cavelier (15352473) (author), Claes Ladenvall (15352476) (author), Panagiotis Baliakas (15352479) (author) |
| منشور في: |
2025
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| الموضوعات: | |
| الوسوم: |
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مواد مشابهة
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Supplementary Table1 from Somatic Exonic Deletions in <i>RUNX1</i> Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
حسب: Anna Eriksson (15352461)
منشور في: (2025) -
Supplementary Appendix S1 from DNA-Methylome–Based Tumor Hypoxia Classifier Identifies HPV-Negative Head and Neck Cancer Patients at Risk for Locoregional Recurrence after Primary Radiochemotherapy
حسب: Bouchra Tawk (15389486)
منشور في: (2025) -
Supplementary Figure 1. from Clinicopathologic, Genomic, and Immunophenotypic Landscape of <i>ATM</i> Mutations in Non–Small Cell Lung Cancer
حسب: Biagio Ricciuti (14951247)
منشور في: (2025) -
Supplementary Figure 10 from Clinicopathologic, Genomic, and Immunophenotypic Landscape of <i>ATM</i> Mutations in Non–Small Cell Lung Cancer
حسب: Biagio Ricciuti (14951247)
منشور في: (2025) -
Supplementary Figure 11 from Clinicopathologic, Genomic, and Immunophenotypic Landscape of <i>ATM</i> Mutations in Non–Small Cell Lung Cancer
حسب: Biagio Ricciuti (14951247)
منشور في: (2025)