Increased copy number at 17q22-q24 by CGH in breast cancer is due to high-level amplification of two separate regions

Genes Chromosomes and Cancer

Volumn 20, Issue 4, 1997, Pages 372-376

  Bärlund, Maarit ^a   Tirkkonen, Mika ^a   Forozan, Farahnaz ^b   Tanner, Minna M ^a   Kallioniemi, Olli ^b   Kallioniemi, Anne ^b  

^a UNIVERSITY OF TAMPERE   (Finland)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; CHROMOSOME 17Q; CHROMOSOME MAP; COMPARATIVE GENOMIC HYBRIDIZATION; COSMID; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE LOCUS; HUMAN; HUMAN CELL; HYBRIDIZATION; INTERPHASE; PRIORITY JOURNAL; TELOMERE;

BREAST NEOPLASMS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DNA PROBES; DNA, NEOPLASM; GENE AMPLIFICATION; GENE DOSAGE; GENES, ERBB-2; GENES, NEOPLASM; GENES, TUMOR SUPPRESSOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; NUCLEIC ACID HYBRIDIZATION; TUMOR CELLS, CULTURED;

EID: 0343196653     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199712)20:4<372::AID-GCC8>3.0.CO;2-Z     Document Type: Article

References (22)

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