Relevance of cytogenetic and fluorescent in situ hybridization analyses in the clinical assessment of soft tissue sarcoma
- 1 February 1997
- journal article
- Published by Elsevier in Human Pathology
- Vol. 28 (2) , 134-142
- https://doi.org/10.1016/s0046-8177(97)90096-4
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Involvement of chromosomes 17 and 22 in dermatofibrosarcoma protuberansGenes, Chromosomes and Cancer, 1995
- Chromosomal translocations in human cancerNature, 1994
- Supernumerary ring chromosomes containing chromosome 17 sequences: A specific feature of dermatofibrosarcoma protuberans?Cancer Genetics and Cytogenetics, 1994
- Complex composition and co‐amplification of SAS and MDM2 in ring and giant rod marker chromosomes in well‐differentiated liposarcomaGenes, Chromosomes and Cancer, 1994
- Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcomaNature Genetics, 1993
- Monoclonal antibodies against recombinant parts of the Ki‐67 antigen (MIB 1 and MIB 3) detect proliferating cells in microwave‐processed formalin‐fixed paraffin sectionsThe Journal of Pathology, 1992
- Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)Genes, Chromosomes and Cancer, 1992
- Interphase cytogenetics for the detection of the t(11;22)(q24;q12) in small round cell tumors.Journal of Clinical Investigation, 1992
- Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumoursNature, 1992
- Chromosomal in situ suppression hybridization after Giemsa bandingHuman Genetics, 1991