Is there still a point for classical cytogenetic banding analysis in the diagnostic work-up of specimens suspicious for lymphoma?

Leukemia and Lymphoma

Volumn 49, Issue 1, 2008, Pages 6-7

  Rosenwald, Andreas ^a   Ott, German ^b  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b ROBERT BOSCH HOSPITAL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

FORMALDEHYDE; PARAFFIN;

CANCER CELL CULTURE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC PROCEDURE; EMBEDDING; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HUMAN; KARYOTYPING; LYMPHOMA; METAPHASE CHROMOSOME; METHODOLOGY; NOTE; PATIENT REFERRAL; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS;

CHROMOSOME BANDING; CYTOGENETIC ANALYSIS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LYMPHOMA; NUCLEIC ACID HYBRIDIZATION;

EID: 38549120166     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.1080/10428190701742514     Document Type: Note

References (4)

1. Dunphy, C. and Tang, W. (2008) Usefulness of routine conventional cytogenetic analysis in tissues submitted for 'lymphoma work-up'. Leuk Lymphoma, 49, pp. 75-80.
2. Haralambieva, E., Kleiverda, K., Mason, D. Y., Schuuring, E. and Kluin, P. M. (2002) Detection of three common translocation breakpoints in non-Hodgkin's lymphomas by fluorescence in situ hybridization on routine paraffin-embedded tissue sections. J Pathol, 198, pp. 163-170.
3. Schwaenen, C., Wessendorf, S., Kestler, H. A., Dohner, H., Lichter, P. and Bentz, M. (2003) DNA microarray analysis in malignant lymphomas. Ann Hematol, 82, pp. 323-332.
4. (2004) An International System for Human Cytogenetics Nomenclature, Karger, Basel