Chromosomal imbalances in a recurrent solitary fibrous tumor of the orbit

Cancer Genetics and Cytogenetics

Volumn 162, Issue 1, 2005, Pages 38-44

  Ness, Gro Oddveig ^a   Lybæk, Helle ^a   Arnes, Jarle ^b   Rødahl, Eyvind ^c  

^a Center for Medical Genetics and Molecular Medicine   (Norway)

^b Department of Pathology ^*

^c HAUKELAND UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANTERIOR CRANIAL FOSSA; ARTICLE; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME 16Q; CHROMOSOME 20P; CHROMOSOME 9P; CHROMOSOME 9Q; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FEMALE; FIBROMA; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MORPHOLOGY; ORBIT TUMOR; PRIORITY JOURNAL; RECURRENT DISEASE; TUMOR CELL;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 9; CRANIAL FOSSA, ANTERIOR; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LOSS OF HETEROZYGOSITY; NEOPLASM RECURRENCE, LOCAL; NEOPLASMS, FIBROUS TISSUE; ORBITAL NEOPLASMS; SKULL BASE NEOPLASMS;

EID: 24644434915     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2005.01.014     Document Type: Article

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