Deletion of 14q24.1∼q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization

Cancer Genetics and Cytogenetics

Volumn 185, Issue 1, 2008, Pages 43-46

  Xu, Weihong ^a   Lu, Xianglan ^a   Kim, YoungMi ^a   Luo, Ying ^a   Martin, Mallory ^a   Mulvihill, John J ^a   Li, Shibo ^a  

^a UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARAGINASE; CYTARABINE; DEXAMETHASONE; TRANSCRIPTION FACTOR ETV6; TRANSCRIPTION FACTOR RUNX1;

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; CASE REPORT; CHROMOSOME 12P; CHROMOSOME 14Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DNA PROBE; ERYTHROCYTE TRANSFUSION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FUSION; HUMAN; HUMAN TISSUE; KARYOTYPE; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL;

CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 14; CYTOGENETIC ANALYSIS; HUMANS; MALE; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA; REMISSION INDUCTION;

ALIAS;

EID: 47549114432     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2008.04.007     Document Type: Article

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