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Volumn 30, Issue 3, 2001, Pages 267-273

Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 3Q; CHROMOSOME 6; CHROMOSOME 7; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPING; PRIORITY JOURNAL; PROGNOSIS; UVEA MELANOMA;

EID: 0035146977     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1088>3.0.CO;2-7     Document Type: Article
Times cited : (61)

References (19)
  • 6
    • 0027506157 scopus 로고
    • Cytogenetic analysis of uveal melanoma: Consistent occurrence of monosomy 3 and trisomy 8q
    • (1993) Cancer , vol.71 , pp. 811-819
    • Horsman, D.E.1    White, V.A.2
  • 10
    • 16044371402 scopus 로고    scopus 로고
    • A complete set of human telomeric probes and their clinical application
    • (1996) Nat Genet , vol.14 , pp. 86-89


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.