The genetics of childhood acute lymphoblastic leukaemia

Bailliere's Best Practice and Research in Clinical Haematology

Volumn 13, Issue 3, 2000, Pages 427-439

  Harrison, Christine J ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Acute lymphoblastic leukaemia; Cytogenetics; Diagnosis; Fluorescence in situ hybridization (FISH); Genes; Genetic changes; Prognosis

Indexed keywords

BCR ABL PROTEIN;

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; CHILD; CHILD CARE; CHILDHOOD LEUKEMIA; CHROMOSOME 12P; CHROMOSOME 19P; CHROMOSOME 1Q; CHROMOSOME 21Q; CHROMOSOME 22Q; CHROMOSOME 6Q; CHROMOSOME 9P; CHROMOSOME 9Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 19; CHROMOSOME TRANSLOCATION 21; CHROMOSOME TRANSLOCATION 22; CHROMOSOME TRANSLOCATION 9; CONTROLLED STUDY; DIAGNOSTIC VALUE; DIPLOIDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUSION; GENE REARRANGEMENT; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; IMMUNOGLOBULIN GENE; INFANT; INTERPHASE; NEWBORN; ONCOGENE MYC; PRIORITY JOURNAL; PROGNOSIS; RISK ASSESSMENT; T LYMPHOCYTE RECEPTOR GENE; TUMOR SUPPRESSOR GENE; UNITED KINGDOM;

EID: 0033677014     PISSN: 15216926     EISSN: None     Source Type: Journal    
DOI: 10.1053/beha.2000.0086     Document Type: Article

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