Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion)

Human Pathology

Volumn 35, Issue 9, 2004, Pages 1063-1069

  Nilsson, Malin ^a   Domanski, Henryk A ^a   Mertens, Fredrik ^a   Mandahl, Nils ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

BAC; bacterial artificial chromosome; basic fibroblastic growth factor; bFGF; bizarre parosteal osteochondromatous proliferation; BPOP; ChM I; chromosome aberration; fluorescence in situ hybridization; Nora's lesion; parosteal chondromatous proliferation

Indexed keywords

ADULT; ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; BIZARRE PAROSTEAL OSTEOCHONDROMATOUS PROLIFERATION; CANCELLOUS BONE; CARTILAGE; CELL COMPOSITION; CHROMOSOME 1; CHROMOSOME 17; CHROMOSOME BANDING PATTERN; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HISTOLOGY; HUMAN; HUMAN CELL; KARYOTYPE; MALE; METAPHASE; OSTEOCHONDROMA; SAMPLE; SIGNAL TRANSDUCTION; SPINDLE CELL;

ADULT; BONE NEOPLASMS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; FINGERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MIDDLE AGED; OSTEOCHONDROMA; TOES; TRANSLOCATION, GENETIC;

EID: 4444319921     PISSN: 00468177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.humpath.2004.02.008     Document Type: Article

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