PMID- 7986725 OWN - NLM STAT- MEDLINE DCOM- 19950109 LR - 20190705 IS - 0007-1048 (Print) IS - 0007-1048 (Linking) VI - 87 IP - 4 DP - 1994 Aug TI - Detection of trisomy 12 in chronic lymphocytic leukaemia: comparison of a polymerase chain reaction based technique with fluorescence in situ hybridization. PG - 843-5 AB - Trisomy 12 is the most frequent chromosomal aberration in chronic lymphocytic leukaemia (CLL) and seems to indicate a poor prognosis. To detect this abnormality we tested the applicability of the polymerase chain reaction (PCR) and compared it to the current standard fluorescence in situ hybridization (FISH). Two DNA regions containing variable numbers of tandem repeats (VNTR) located on (a) the long and (b) the short arm of chromosome 12 were chosen for PCR analysis. 8/72 patients (11%) were trisomy 12 positive compared to 16% by FISH. Chromosomal imbalances were only detected by PCR if at least 20% of the cells carried the numerical aberration. FAU - Reining, G AU - Reining G AD - Clinical Institute of Medical and Chemical Laboratory Diagnosis, University of Vienna, Austria. FAU - Clodi, K AU - Clodi K FAU - Konig, M AU - Konig M FAU - Geissler, K AU - Geissler K FAU - Haas, O A AU - Haas OA FAU - Mannhalter, C AU - Mannhalter C LA - eng PT - Comparative Study PT - Journal Article PL - England TA - Br J Haematol JT - British journal of haematology JID - 0372544 SB - IM MH - *Chromosomes, Human, Pair 12 MH - Gene Dosage MH - Humans MH - *In Situ Hybridization, Fluorescence MH - Leukemia, Lymphocytic, Chronic, B-Cell/*genetics MH - *Polymerase Chain Reaction MH - Sensitivity and Specificity MH - *Trisomy EDAT- 1994/08/01 00:00 MHDA- 1994/08/01 00:01 CRDT- 1994/08/01 00:00 PHST- 1994/08/01 00:00 [pubmed] PHST- 1994/08/01 00:01 [medline] PHST- 1994/08/01 00:00 [entrez] AID - 10.1111/j.1365-2141.1994.tb06748.x [doi] PST - ppublish SO - Br J Haematol. 1994 Aug;87(4):843-5. doi: 10.1111/j.1365-2141.1994.tb06748.x.