Coamplification of 12p11 and 12q13∼q22 in multiple ring chromosomes in a spindle cell sarcoma resolved by novel multicolor fluorescence in situ hybridization analysis

Cancer Genetics and Cytogenetics

Volumn 139, Issue 1, 2002, Pages 44-47

  Lestou, Valia S ^a,b   O'Connell, John X ^c   Ludkovski, Olga ^a   Gosling, Helena ^a   Lesack, David ^d   Horsman, Douglas E ^a,b  

^a BRITISH COLUMBIA CANCER AGENCY   (Canada)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c SURREY MEMORIAL HOSPITAL   (Canada)

^d KELOWNA GENERAL HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ANAPHASE; ARTICLE; CANCER DIAGNOSIS; CASE REPORT; CHROMOSOME 12; CHROMOSOME 12P; CHROMOSOME 12Q; CHROMOSOME 18; CHROMOSOME ANALYSIS; CLINICAL FEATURE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENETIC HETEROGENEITY; HUMAN; HUMAN TISSUE; KARYOTYPE; MALE; PRIORITY JOURNAL; SPINDLE CELL SARCOMA;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 9; GENE AMPLIFICATION; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MIDDLE AGED; RING CHROMOSOMES; SARCOMA;

EID: 0036874586     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(02)00600-3     Document Type: Article

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