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Cancer Genetics and Cytogenetics

Volumn 131, Issue 1, 2001, Pages 82-85

Isochromosome (17)(q10) and translocation (4;12)(q12;p13) in a child with acute myeloid leukemia

(4) Nathan, Paul C a Chun, Kathy b Abdelhaleem, Mohamed a,c Malkin, David a

a Division of Haematology/Oncology (Canada)

b UNIVERSITY OF TORONTO (Canada)

c HOSPITAL FOR SICK CHILDREN (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ARTICLE; BONE MARROW; CASE REPORT; CHROMOSOME 12P; CHROMOSOME 12Q; CHROMOSOME 17Q; CHROMOSOME TRANSLOCATION; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; ISOCHROMOSOME; KARYOTYPE; PRIORITY JOURNAL;

ADOLESCENT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOCHROMOSOMES; KARYOTYPING; LEUKEMIA, MYELOCYTIC, ACUTE; TRANSLOCATION, GENETIC;

EID: 0035176385 PISSN: 01654608 EISSN: None Source Type: Journal
DOI: 10.1016/S0165-4608(01)00494-0 Document Type: Article

Times cited : (5)

References (11)

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2
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