Detection of the Der (21)t(12;21) Chromosome Forming the TEL-AML1 Fusion Gene in Childhood Acute Lymphoblastic Leukemia

Leukemia and Lymphoma

Volumn 28, Issue 42006, 1997, Pages 43-50

  Kobayashi, Hirofumi ^a   Satake, Noriko ^a   Kaneko, Yasuhiko ^a  

^a SAITAMA CANCER CENTER   (Japan)

Author keywords

ALL; AML1; chromosomal aberration; TEL

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ADULT; AGE; ASIAN; B LYMPHOCYTE; CANCER RECURRENCE; CAUCASIAN; CHILD; CHILDHOOD LEUKEMIA; CHROMOSOME 12P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FUSION; HUMAN; HUMAN CELL; IMMUNOPHENOTYPING; INTERPHASE; LEUKEMIA CELL; LEUKEMOGENESIS; MAJOR CLINICAL STUDY; MYELOID LEUKEMIA; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; REVIEW; SCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 21; CORE BINDING FACTOR ALPHA 2 SUBUNIT; HUMANS; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; NEOPLASM PROTEINS; ONCOGENE PROTEINS, FUSION; TRANSLOCATION, GENETIC; TUMOR MARKERS, BIOLOGICAL;

EID: 0031426612     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.3109/10428199709058329     Document Type: Article

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