A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay

Blood

Volumn 99, Issue 7, 2002, Pages 2526-2531

  Brown, Jill ^a,b   Jawad, Mays ^a,b   Twigg, Stephen R F ^a,b   Saracoglu, Kaan ^a,b   Sauerbrey, Axel ^a,b   Thomas, Angela E ^a,b   Eils, Roland ^a,b   Harbott, Jochen ^a,b   Kearney, Lyndal ^a,b  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ANALYTIC METHOD; ARTICLE; ASSAY; CASE REPORT; CHILD; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 5; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUSION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; TELOMERE;

EID: 0036530203     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V99.7.2526     Document Type: Article

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