Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization

Genes Chromosomes and Cancer

Volumn 23, Issue 3, 1998, Pages 203-212

  Gisselsson, David ^a   Höglund, Mattias ^a   Mertens, Fredrik ^a   Mitelman, Felix ^a   Mandahl, Nils ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 12; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME STRUCTURE; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE SEQUENCE; HETEROCHROMATIN; HISTOPATHOLOGY; HUMAN; HUMAN CELL; KARYOTYPING; MALE; MESENCHYMOMA; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TELOMERE;

ADOLESCENT; ADULT; CHROMOSOME BANDING; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 12; DNA, SATELLITE; FEMALE; FIBROSARCOMA; GENE AMPLIFICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MIDDLE AGED; NEOPLASMS, ADIPOSE TISSUE; OSTEOSARCOMA; PHYSICAL CHROMOSOME MAPPING; RING CHROMOSOMES;

EID: 0345676507     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199811)23:3<203::AID-GCC1>3.0.CO;2-5     Document Type: Article

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