Genetic lesions in a preleukemic aplasia phase in a child with acute lymphoblastic leukemia

Genes Chromosomes and Cancer

Volumn 47, Issue 4, 2008, Pages 333-340

  Horsley, Sharon W ^a   Colman, Susan ^a   McKinley, Mark ^b,d   Bateman, Caroline M ^a   Jenney, Meriel ^b   Chaplin, Tracy ^c   Young, Bryan D ^c   Greaves, Mel ^a   Kearney, Lyndal ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

^c QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^d QML Pathology   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; APLASTIC ANEMIA; ARTICLE; BLOOD; BONE MARROW; CASE REPORT; ETV6 RUNX1 FUSION GENE; FLUORESCENCE IN SITU HYBRIDIZATION; FUSION GENE; GENETIC DISORDER; GENOTYPE; HETEROZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM;

ANEMIA, APLASTIC; BONE MARROW; CHILD, PRESCHOOL; CORE BINDING FACTOR ALPHA 2 SUBUNIT; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MICROARRAY ANALYSIS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; ONCOGENE PROTEINS, FUSION; POLYMORPHISM, SINGLE NUCLEOTIDE; PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA; PRELEUKEMIA; RETROSPECTIVE STUDIES;

EID: 40049102287     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.20537     Document Type: Article

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