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Paper Details

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood <i>ETV6::RUNX1+</i> and High Hyperdiploid Acute Lymphoblastic Leukemia.
Hemasphere
2
2023
+, 10p14, 12p13, 12q24.21, 18q11, 1p34, 20q11.22, 4q24, 8p11, 8p23, 9p21, B, B-cell precursor acute lymphoblastic leukemia, BCP-ALL, Childhood, HD BCP-ALL, High Hyperdiploid Acute Lymphoblastic Leukemia, SNP, SNVs, SVs, fusion genes, leukemia, patient, patients, pediatric cancer, recurrently altered regions, single nucleotide polymorphism (SNP) array, single-nucleotide variants
Author NameAffiliation
Daniel PicardHematology and Clinical Immunology, Heinrich-Heine University and University Hospital Dusseldorf
Tobias MarschallInstitute for Medical Biometry and Bioinformatics, Heinrich-Heine University
Tobias MarschallCenter for Digital Medicine, Heinrich-Heine University
Arndt BorkhardtHematology and Clinical Immunology, Heinrich-Heine University and University Hospital Dusseldorf
Arndt Borkhardt
Arndt BorkhardtHematology and Clinical Immunology, Heinrich-Heine University and University Hospital Dusseldorf
Arndt Borkhardt
Ute FischerHematology and Clinical Immunology, Heinrich-Heine University and University Hospital Dusseldorf
Ute Fischer
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