Marie Engvall
0000-0002-7394-9191
9 papers found
Refreshing results…
Supplementary Table1 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
Data from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
Supplementary Data 1 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
Supplementary Table 2 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
Supplementary Table 1 from Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
Familial platelet disorder due to germline exonic deletions inRUNX1: a diagnostic challenge with distinct alterations of the transcript isoform equilibrium
Challenging conventional karyotyping by next-generation karyotyping in 281 intensively treated patients with AML
Detection of leukemia gene fusions by targeted RNA-sequencing in routine diagnostics
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