Chromosome 11q deletion in myeloid malignancies

Leukemia

Volumn 16, Issue 5, 2002, Pages 953-955

  Ma, S K ^a   Wan, T S K ^a   Au, W Y ^a   Fung, L F ^a   So, C K ^a   Chan, L C ^a  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ALLELE; CHILD; CHROMOSOME 11Q; CHROMOSOME 20Q; CHROMOSOME 5; CHROMOSOME 7; CHROMOSOME 9Q; CHROMOSOME ARM; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DIAGNOSTIC TEST; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOSS; HUMAN; KARYOTYPE; LETTER; LEUKEMOGENESIS; MALE; MYELODYSPLASTIC SYNDROME; MYELOID LEUKEMIA; PREVALENCE; PRIORITY JOURNAL; PROGNOSIS; TUMOR SUPPRESSOR GENE;

EID: 0036110423     PISSN: 08876924     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.leu.2402442     Document Type: Letter

References (9)

1. The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1612 patients entered into the MRC AML 10 trial
2. International scoring system for evaluating prognosis in myelodysplastic syndromes
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4. Chromosome 20 deletions in myeloid malignancies: Reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes
5. Abnormalities of the long arm of chromosome 11 (11q) in patients with de novo and secondary acute myelogenous leukemias and myelodysplastic syndromes
6. Hematological malignancies with a deletion of 11q23: Cytogenetic and clinical aspects
7. Characterization of additional genetic events in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion: A molecular cytogenetics study
8. Analysis of deletions of the long arm of chromosome 11 in hematologic malignancies with fluorescence in situ hybridization
9. Altered Hox expression and segmental identity in MII-mutant mice