Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type region: Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics

American Journal of Pathology

Volumn 155, Issue 1, 1999, Pages 61-66

  Gisselsson, David ^a   Höglund, Mattias ^a   Mertens, Fredrik ^a   Dal Cin, Paola ^b   Mandahl, Nils ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BROWN ADIPOSE TISSUE; CHROMOSOME 11Q; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; COSMID VECTOR; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; HETEROZYGOSITY LOSS; HIBERNOMA; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0345004941     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9440(10)65099-7     Document Type: Article

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