A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines

Cancer Genetics and Cytogenetics

Volumn 110, Issue 2, 1999, Pages 82-86

  Magnani, Ivana ^a   Chiariello, Elena ^b   Conti, Anna Maria Fuhrman ^a   Finocchiaro, Gaetano ^b  

^a UNIVERSITY OF MILAN   (Italy)

^b DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN TUMOR; CHROMOSOME 19Q; CHROMOSOME REARRANGEMENT; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GLIOBLASTOMA; HUMAN; HUMAN CELL; PRIORITY JOURNAL; TUMOR CELL;

BRAIN NEOPLASMS; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 19; GLIOBLASTOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; TRANSLOCATION, GENETIC; TUMOR CELLS, CULTURED;

EID: 0033561103     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00190-3     Document Type: Article

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