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Two genetic pathways,t(1;10) and amplification of 3p11–12, in myxoinflammatory fibroblastic sarcoma,haemosiderotic fibrolipomatous tumour,and morphologically similar lesions
Authors:Karolin H Hallor,Raf Sciot,Johan Staaf,Markus Heidenblad,Anders Rydholm,Henrik CF Bauer,Kristina   str  m,Henryk A Domanski,Jeanne M Meis,Lars‐Gunnar Kindblom,Ioannis Panagopoulos,Nils Mandahl,Fredrik Mertens
Affiliation:1. Department of Clinical Genetics, University Hospital, Lund, Sweden;2. Department of Pathology, Catholic University of Leuven, Leuven, Belgium;3. Department of Oncology, University Hospital, Lund, Sweden;4. Department of Orthopedics, University Hospital, Lund, Sweden;5. Department of Orthopedics, Karolinska Hospital, Stockholm, Sweden;6. Department of Pathology, Karolinska Hospital, Stockholm, Sweden;7. Department of Pathology, University Hospital, Lund, Sweden;8. Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA;9. Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, UK
Abstract:
Keywords:myxoinflammatory fibroblastic sarcoma  haemosiderotic fibrolipomatous tumour  inflammatory malignant fibrous histiocytoma  FGF8  NPM3  TGFBR3  VGLL3  t(1  10)  ring chromosome
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