Delineation of the frequently deleted region on chromosome arm 13q in B-cell non-Hodgkin's lymphoma

International Journal of Hematology

Volumn 71, Issue 2, 2000, Pages 159-166

  Wada, Makio ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

13q deletion; B cell non hodgkin's lymphoma; Chronic lymphocytic leukemia; Loss of heterozygosity; Tumor suppressor gene

Indexed keywords

MICROSATELLITE DNA;

ADULT; AGED; ARTICLE; B CELL LYMPHOMA; CHROMOSOME 13; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DISORDER; CHROMOSOME MAP; FEMALE; GENE DELETION; GENETICS; HETEROZYGOSITY LOSS; HUMAN; MALE; MIDDLE AGED; TUMOR SUPPRESSOR GENE;

ADULT; AGED; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; CYTOGENETIC ANALYSIS; FEMALE; GENE DELETION; GENES, TUMOR SUPPRESSOR; HUMANS; LOSS OF HETEROZYGOSITY; LYMPHOMA, B-CELL; MALE; MICROSATELLITE REPEATS; MIDDLE AGED;

EID: 0034136475     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (2)

1. Chappuis PO, Sappino A-P. Lymphoid neoplasms - molecular characterizations of non-Hodgkin's lymphomas: Impact on patient management. Semin Hematol. 1995:32:237-241.
2. Raffeld M, Yano T. Molecular pathogenesis of B-cell lymphomas: an overview. In: Kurzrock R, Talpaz M., eds. Molecular Biology in Cancer Medicine. London, Martin Dunitz:1995;196-211.