Loss of chromosome 13 is the most frequent genomic imbalance in malignant fibrous histiocytomas: A comparative genomic hybridization analysis of a series of 30 cases

Cancer Genetics and Cytogenetics

Volumn 111, Issue 2, 1999, Pages 134-138

  Mairal, Aline ^a   Terrier, Philippe ^b   Chibon, Frédéric ^a   Sastre, Xavier ^a   Lecesne, Axel ^b   Aurias, Alain ^a  

^a INSTITUT CURIE   (France)

^b INSTITUT GUSTAVE ROUSSY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER RECURRENCE; CARCINOGENESIS; CHROMOSOME 13; CHROMOSOME LOSS; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; GENE LOCUS; HUMAN; HUMAN TISSUE; MALIGNANT FIBROUS HISTIOCYTOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; DNA, NEOPLASM; HISTIOCYTOMA, BENIGN FIBROUS; HUMANS; IN SITU HYBRIDIZATION; METAPHASE; NEOPLASM RECURRENCE, LOCAL; SOFT TISSUE NEOPLASMS; X CHROMOSOME;

EID: 0032901704     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00227-1     Document Type: Article

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