The 12;21 translocation involving TEL and deletion of the other TEL allele: Two frequently associated alterations found in childhood acute lymphoblastic leukemia

Blood

Volumn 87, Issue 7, 1996, Pages 2891-2899

  Raynaud, Sophie ^b   Cavé, Hélène ^b   Baens, Mathijs ^b   Bastard, Christian ^b   Cacheux, Valère ^b   Grosgeorge, Josiane ^b   Guidal Giroux, Christine ^b   Guo, Caiying ^b   Vilmer, Etienne ^b   Marynen, Peter ^b   Grandchamp, Bernard ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ALLELE; ARTICLE; CHILD; CHILDHOOD LEUKEMIA; CHROMOSOME 12P; CHROMOSOME DELETION; CHROMOSOME LOSS; CHROMOSOME SATELLITE; CHROMOSOME TRANSLOCATION 12; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUSION; HUMAN; HUMAN CELL; INFANT; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; NEWBORN; PRIORITY JOURNAL;

EID: 9244221153     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v87.7.2891.bloodjournal8772891     Document Type: Article

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