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Volumn 92, Issue 2, 1996, Pages 389-392

Trisomy 12 and structural abnormalities of 13q14 occurring in the same clone in chronic lymphocytic leukaemia

Author keywords

Chromosome 13q14 abnormalities; Chronic lymphocytic leykaemia; Cytogenetics; Fluorescence in situ hybridization; Trisomy 12

Indexed keywords

ADULT; AGED; ARTICLE; CELL STRUCTURE; CHROMOSOME 12; CHROMOSOME 13; CHROMOSOME DAMAGE; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ARTICLE; CYTOGENETICS; FEMALE; HUMAN; IN SITU HYBRIDIZATION; KARYOTYPE; MALE; PRIORITY JOURNAL; TRISOMY;

EID: 0030039406     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1996.d01-1492.x     Document Type: Article
Times cited : (36)

References (13)
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  • 6
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    • Hawthorn, L.A., Chapman, R., Oscier, D. & Cowell, J. (1993) The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene. Oncogene, 8, 1415-1419.
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  • 9
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.