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Volumn 123, Issue 2, 2000, Pages 97-101
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Detection of t(14;18)(q32;q21) in hyperdiploid cells by fluorescence in situ hybridization in a patient with Hodgkin disease
a b b c d e f a |
Author keywords
[No Author keywords available]
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Indexed keywords
BUSULFAN;
CD30 ANTIGEN;
CYCLOPHOSPHAMIDE;
CYTARABINE;
ETOPOSIDE;
MITOXANTRONE;
PROTEIN BCL 2;
ARTICLE;
CASE REPORT;
CELL STRUCTURE;
CERVICAL LYMPH NODE;
CHEMOTHERAPY;
COMPUTER ASSISTED TOMOGRAPHY;
CYTOGENETICS;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE TRANSLOCATION;
HODGKIN DISEASE;
HUMAN;
HUMAN CELL;
IMMUNOHISTOCHEMISTRY;
LYMPH NODE BIOPSY;
LYMPHADENOPATHY;
MALE;
PERIPHERAL BLOOD STEM CELL;
PRIORITY JOURNAL;
REED STERNBERG CELL;
STEM CELL TRANSPLANTATION;
THERAPY RESISTANCE;
ADULT;
ANEUPLOIDY;
CHROMOSOMES, HUMAN, PAIR 14;
CHROMOSOMES, HUMAN, PAIR 18;
HODGKIN DISEASE;
HUMANS;
IMMUNOHISTOCHEMISTRY;
IN SITU HYBRIDIZATION, FLUORESCENCE;
MALE;
PROTO-ONCOGENE PROTEINS C-BCL-2;
TRANSLOCATION, GENETIC;
PHRAGMITES;
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EID: 0034541539
PISSN: 01654608
EISSN: None
Source Type: Journal
DOI: 10.1016/S0165-4608(00)00311-3 Document Type: Article |
Times cited : (6)
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References (22)
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