Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas

Cancer

Volumn 82, Issue 9, 1998, Pages 1657-1663

  Bridge, Julia A ^a,c   Nelson, Mari ^a   Örndal, Charlotte ^a   Bhatia, Paramjit ^b   Neff, James R ^a  

^a UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^b UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

^c UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

Author keywords

Chromosome; Cytogenetic; Exostoses; Karyotype; Osteochondroma

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CANCER GENETICS; CHILD; CHROMOSOME 11P; CHROMOSOME 8Q; CHROMOSOME ANALYSIS; CHROMOSOME LOSS; CLINICAL ARTICLE; FAMILIAL CANCER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; GENE MUTATION; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; KARYOTYPE; MALE; OSTEOCHONDROMA; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 8; EXOSTOSES, MULTIPLE HEREDITARY; FEMALE; GENE REARRANGEMENT; HUMANS; KARYOTYPING; MALE; OSTEOCHONDROMA;

EID: 0032080482     PISSN: 0008543X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0142(19980501)82:9<1657::AID-CNCR10>3.0.CO;2-3     Document Type: Article

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