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Volumn 97, Issue 4, 1997, Pages 844-847

Lack of clonal BCRA2 gene deletion on chromosome 13 in chronic lymphocytic leukaemia

Author keywords

13q12; 13q14; Chromosomal abnormality; CLL; Clonality

Indexed keywords

ARTICLE; CHROMOSOME 13Q; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; GENE DELETION; GENE LOCATION; HUMAN; PRIORITY JOURNAL; PROTO ONCOGENE; TUMOR SUPPRESSOR GENE;

EID: 0030769460     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1997.1322949.x     Document Type: Article
Times cited : (16)

References (12)
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  • 2
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    • Frequent somatic deletion of the 13q12.3 locus encompassing BRCA2 in chronic lymphocytic leukemia
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  • 6
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    • The consistent 13q14 translocation breakpoint seen in chronic B-cell leukemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene
    • Hawthorn, L.A., Chapman, R., Oscier, D.G. & Cowell, J.K. (1993) The consistent 13q14 translocation breakpoint seen in chronic B-cell leukemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene. Oncogene, 8, 1415-1419.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.