Fluorescence in situ hybridization mapping of breakpoints in pleomorphic adenomas with 8q12-13 abnormalities identifies a subgroup of tumors without PLAGI involvement

Genes Chromosomes and Cancer

Volumn 24, Issue 1, 1999, Pages 78-82

  Röijer, Eva ^a   Kas, Koen ^b   Behrendt, Margareta ^a   Van De Ven, Wim ^b   Stenman, Göran ^a,c  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 8Q; CHROMOSOME BREAKAGE; CHROMOSOME INSERTION; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE MAPPING; GENE REARRANGEMENT; HUMAN; NORTHERN BLOTTING; PLEOMORPHIC ADENOMA; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; YEAST ARTIFICIAL CHROMOSOME;

ADENOMA, PLEOMORPHIC; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKAGE; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 8; DNA-BINDING PROTEINS; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; TRANSLOCATION, GENETIC; ZINC FINGERS;

EID: 0032889642     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199901)24:1<78::AID-GCC11>3.0.CO;2-D     Document Type: Article

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