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Volumn 37, Issue 8, 2013, Pages 928-935

Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia

Author keywords

CI FISH; Driving molecular lesions; GEP; Paediatric T ALL; Secondary events; SNP

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ARTICLE; CANCER CLASSIFICATION; CANCER PATIENT; CANCER PROGNOSIS; CHILD; CHILDHOOD LEUKEMIA; CLINICAL TRIAL; COMBINED INTERPHASE FLUORESCENCE IN SITU HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE EXPRESSION PROFILING; GENETIC DISORDER; GENETIC LINKAGE; HOXA GENE; HUMAN; LMO GENE; MAJOR CLINICAL STUDY; MALE; MINIMAL RESIDUAL DISEASE; MOLECULAR DIAGNOSIS; NKX2 1 GENE; PATIENT CODING; PERSONALIZED MEDICINE; PREDICTION; PRIORITY JOURNAL; RISK ASSESSMENT; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; T CELL LEUKEMIA; TAL GENE; TLX1 GENE; TLX3 GENE;

EID: 84879784602     PISSN: 01452126     EISSN: 18735835     Source Type: Journal    
DOI: 10.1016/j.leukres.2013.04.005     Document Type: Article
Times cited : (16)

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