Novel Chromosome 16 abnormality-der(16)del(16)(q13)t(16;21)(p11.2;q22) - Associated with acute myeloid leukemia

Cancer Genetics and Cytogenetics

Volumn 113, Issue 1, 1999, Pages 25-28

  Sharma, P ^a   Watson, N ^a   Robson, L ^a   Gallo, J ^b   Smith, A ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b LIVERPOOL HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; AGED; ARTICLE; CASE REPORT; CHROMOSOME 16; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MALE; METAPHASE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

AGED; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 21; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOCYTIC, ACUTE; MALE; MYELODYSPLASTIC SYNDROMES; TRANSLOCATION, GENETIC;

EID: 0032839094     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00008-4     Document Type: Article

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