000 01332 a2200361 4500
005 20250513175304.0
264 0 _c19990507
008 199905s 0 0 eng d
022 _a0165-4608
024 7 _a10.1016/s0165-4608(98)00190-3
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMagnani, I
245 0 0 _aA recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines.
_h[electronic resource]
260 _bCancer genetics and cytogenetics
_cApr 1999
300 _a82-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBrain Neoplasms
_xgenetics
650 0 4 _aChromosome Aberrations
650 0 4 _aChromosome Banding
650 0 4 _aChromosome Breakage
650 0 4 _aChromosomes, Human, Pair 19
650 0 4 _aGlioblastoma
_xgenetics
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aKaryotyping
650 0 4 _aTranslocation, Genetic
650 0 4 _aTumor Cells, Cultured
700 1 _aChiariello, E
700 1 _aConti, A M
700 1 _aFinocchiaro, G
773 0 _tCancer genetics and cytogenetics
_gvol. 110
_gno. 2
_gp. 82-6
856 4 0 _uhttps://doi.org/10.1016/s0165-4608(98)00190-3
_zAvailable from publisher's website
999 _c10173581
_d10173581