ETV6-RUNX1 fusion gene and additional genetic changes in infant leukemia: a genome-wide analysis

Cancer Genetics and Cytogenetics

Volumn 193, Issue 2, 2009, Pages 86-92

  Emerenciano, Mariana ^a   Bungaro, Silvia ^b   Cazzaniga, Giovanni ^b   Dorea, Maria Dolores Fonseca ^c   Coser, Virginia Maria ^d   Magalhães, Isis Quezado ^e   Biondi, Andrea ^b   Pombo de Oliveira, Maria S ^a  

^a INSTITUTO NACIONAL DE CÂNCER   (Brazil)

^b UNIVERSITY OF MILANO BICOCCA   (Italy)

^c Oncology Society ClínicaOnco   (Brazil)

^d University of Santa Maria   (Brazil)

^e SES DF   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR ETV6; TRANSCRIPTION FACTOR RUNX1;

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ARTICLE; CHILD; CHILD HEALTH; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 21; CLINICAL ARTICLE; FEMALE; FUSION GENE; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; INFANT; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CHILD; CHILD, PRESCHOOL; CORE BINDING FACTOR ALPHA 2 SUBUNIT; FEMALE; GENE FUSION; GENOME-WIDE ASSOCIATION STUDY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; ONCOGENE PROTEINS, FUSION; POLYMORPHISM, SINGLE NUCLEOTIDE; PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;

EID: 68049100410     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2009.04.021     Document Type: Article

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