A t(1;9)(q23.3∼q25;q34) affecting the ABL1 gene in a biphenotypic leukemia

Cancer Genetics and Cytogenetics

Volumn 152, Issue 1, 2004, Pages 81-83

  González García, Juan Ramón ^a   Bohlander, Stefan K ^b   Gutiérrez Angulo, Melva ^a,c   Esparza Flores, María Amparo ^d   Picos Cárdenas, Verónica Judith ^a,c   Meza Espinoza, Juan Pablo ^a,c   Ayala Madrigal, María De La Luz ^a,c   Rivera, Horacio ^a  

^a INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

^c UNIVERSITY OF GUADALAJARA   (Mexico)

^d HOSPITAL DE PEDIATRÍA   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

ABL1 GENE; ADOLESCENT; ARTICLE; BIPHENOTYPIC LEUKEMIA; CASE REPORT; CHROMOSOME 1; CHROMOSOME 9; CHROMOSOME TRANSLOCATION; DNA FLANKING REGION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE FUSION; GENE LOCUS; HUMAN; LEUKEMIA; MALE; ONCOGENE; PBX1 GENE; PRIORITY JOURNAL;

ADOLESCENT; ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 9; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEUKEMIA; MALE; PHENOTYPE; PROTO-ONCOGENE PROTEINS C-ABL; SENSITIVITY AND SPECIFICITY; TRANSLOCATION, GENETIC;

EID: 2942614881     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2003.10.014     Document Type: Article

References (13)

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