Co-existence of multiple subclones in TEL-AML1 at diagnosis of acute lymphoblastic leukaemia in association with submicroscopic deletion of AML1

Keyphrases

• Acute Lymphoblastic Leukemia 100%
• Subclone 100%
• TEL-AML1 100%
• Submicroscopic Deletion 100%
• AML1 100%
• Working Diagnosis 100%
• TCR Gene Rearrangement 20%
• Differential Response 20%
• Fluorescence in Situ Hybridization 20%
• Polymerase Chain Reaction 20%
• Multi-parameter 20%
• Low Risk 20%
• Delayed Diagnosis 20%
• Leukemia 20%
• Relapse Rate 20%
• Bone Marrow Cells 20%
• Clonal Evolution 20%
• Reaction Studies 20%
• Pediatric Patients 20%
• Fusion Gene 20%
• Trisomy 21 20%
• Response to Chemotherapy 20%
• TEL-AML1 Fusion Gene 20%
• Pediatric Acute Lymphoblastic Leukemia 20%
• ETV6-RUNX1 Fusion 20%
• Interphase Fluorescence in Situ Hybridization 20%
• Additional Chromosomal Abnormalities 20%
• Tetrasomy 21 20%
• Genetic Rearrangement 20%

Biochemistry, Genetics and Molecular Biology

• Fluorescence in Situ Hybridization 100%
• Fusion Gene 100%
• Genetics 50%
• Trisomy 50%
• Chromosomal Abnormalities 50%
• T-Cell Gene Rearrangement 50%
• Polymerase Chain Reaction 50%
• Clonal Evolution 50%
• ETV6 50%
• RUNX1 50%
• Tetrasomy 50%
• Interphase 50%

Medicine and Dentistry

• Acute Lymphoblastic Leukemia 100%
• Fluorescence in Situ Hybridization 40%
• Fusion Gene 40%
• Polymerase Chain Reaction 20%
• Pediatrics 20%
• Recurrence Risk 20%
• Chromosome Aberration 20%
• Trisomy 20%
• Pediatrics Patient 20%
• Interphase 20%
• Tetrasomy 20%
• T-Cell Gene Rearrangement 20%
• Leukemia 20%
• Bone Marrow Cell 20%