EWS/FLI-1 fusion signal inserted into chromosome 11 in one patient with morphologic features of Ewing sarcoma, but lacking t(11;22)
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference16 articles.
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2. The Ewing family of tumors-a subgroup of small-round-cell tumors defined by specific chimeric transcripts;Delattre;N Engl J Med,1994
3. A variant Ewing's sarcoma translocation (7;22) fuses the EWS gene to the ETS gene ETV1;Jeon;Oncogene,1995
4. Fusion of an ETS-family gene, EIAF, to EWS by t(17;22)(q12;q12) chromosome translocation in an undifferentiated sarcoma of infancy;Kaneko;Genes Chromosomes Cancer,1996
5. Updates on cytogenetics and molecular genetics of bone and soft tissue tumors;Sandberg;Cancer Genet Cytogenet,2000
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1. A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD);Cytogenetic and Genome Research;2020
2. Molecular pathology of bone tumours: diagnostic implications;Histopathology;2013-10-31
3. Integrated multimodal genetic testing of Ewing sarcoma—a single-institution experience;Human Pathology;2013-10
4. Cryptic deletion of EGR1 in association with a novel balanced t(5;22)(q31;q11.2) in a patient with myelodysplastic syndrome;Cancer Genetics and Cytogenetics;2009-06
5. Cryptic chromosome rearrangement resulting in SYT-SSX2 fusion gene in a monophasic synovial sarcoma;Cancer Genetics and Cytogenetics;2008-11
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