Polysomy 13 with concomitant deletion of 13q13-14 involving the retinoblastoma gene and the D13S25 locus in a case of acute myeloid leukemia

Cancer Genetics and Cytogenetics

Volumn 119, Issue 2, 2000, Pages 158-161

  Stefanova, Margarita ^a   Dierlamm, Judith ^a   Michaux, Lucienne ^b   Leberecht, Petra ^a   Seeger, Doris ^a   Hinz, Kristina ^a   Hossfeld, Dieter Kurt ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; ARTICLE; CASE REPORT; CHROMOSOME 13; CHROMOSOME 7; CHROMOSOME DELETION 13; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MALE; PRIORITY JOURNAL; TRISOMY 13; TUMOR SUPPRESSOR GENE;

AGED; ANEUPLOIDY; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 7; CLONE CELLS; FATAL OUTCOME; GENE AMPLIFICATION; GENES, RETINOBLASTOMA; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOMONOCYTIC, ACUTE; MALE; TRANSLOCATION, GENETIC; TUMOR STEM CELLS;

EID: 0034097001     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00230-7     Document Type: Article

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