2001
DOI: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1088>3.0.co;2-7
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Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization

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Cited by 61 publications

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“…Table 2 shows the chromosomal changes for all 18 tumours analysed, and Figure 2 shows the frequency of CNAs detected at the level of each chromosome arm. The overall frequency of alterations observed in the 18 tumours was higher than has been previously reported in metaphase CGH studies of UVM (Ghazvini et al, 1996;Tschentscher et al, 2000;Aalto et al, 2001;Naus et al, 2001). This reflects the greater sensitivity of array CGH.…”
Section: Results
mentioning
confidence: 49%