Aberrations of chromosomes 5 and 8 as recurrent cytogenetic events in anaplastic carcinoma of the thyroid as detected by fluorescence in situ hybridisation and comparative genomic hybridisation

Virchows Archiv

Volumn 436, Issue 4, 2000, Pages 312-318

  Wilkens, Ludwig ^a   Benten, Daniel ^a   Tchinda, Joelle ^a   Brabant, Georg ^a   Pötter, Eyck ^a   Dralle, Henning ^b   Von Wasielewski, Reinhard ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b NONE

Author keywords

Anaplastic carcinoma; CGH; Cytogenetics; FISH; Thyroid

Indexed keywords

DNA;

ADULT; AGED; ANAPLASTIC CARCINOMA; ARTICLE; CHROMOSOME 11P; CHROMOSOME 11Q; CHROMOSOME 12Q; CHROMOSOME 14; CHROMOSOME 15; CHROMOSOME 17Q; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME 20Q; CHROMOSOME 21P; CHROMOSOME 3Q; CHROMOSOME 4Q; CHROMOSOME 5; CHROMOSOME 5P; CHROMOSOME 7P; CHROMOSOME 7Q; CHROMOSOME 8P; CHROMOSOME 8Q; CHROMOSOME 9Q; CHROMOSOME LOSS; CHROMOSOME XP; CHROMOSOME XQ; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; NUMERICAL CHROMOSOME ABERRATION; PRIORITY JOURNAL; THYROID CARCINOMA;

EID: 0034090225     PISSN: 09456317     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004280050452     Document Type: Article

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