Fusion gene profile of biphenotypic sinonasal sarcoma: an analysis of 44 cases
Author:
Affiliation:
1. Department of Laboratory Medicine and Pathology; Mayo Clinic; Rochester MN USA
2. Department of Orthopedic Surgery; Mayo Clinic; Rochester MN USA
3. Department of Pathology and Laboratory Medicine; University of Pennsylvania; Philadelphia PA USA
Publisher
Wiley
Subject
General Medicine,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/his.13045/fullpdf
Reference10 articles.
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2. Recurrent PAX3-MAML3 fusion in biphenotypic sinonasal sarcoma;Wang;Nat. Genet.,2014
3. Novel PAX3-NCOA1 fusions in biphenotypic sinonasal sarcoma with focal rhabdomyoblastic differentiation;Huang;Am. J. Surg. Pathol.,2015
4. Alternate PAX3-FOXO1 oncogenic fusion in biphenotypic sinonasal sarcoma;Wong;Genes Chromosomes Cancer,2016
5. Two novel translocations, t(2;4)(q35;q31) and t(X;12)(q22;q24), as the only karyotypic abnormalities in a malignant peripheral nerve sheath tumor of the skull base;Gil;Cancer Genet. Cytogenet.,2003
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