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- 2020
-
Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
(
- Contribution to journal › Article
- 2019
-
Mark
PRDM10 -rearranged Soft Tissue Tumor : A Clinicopathologic Study of 9 Cases
(
- Contribution to journal › Article
- 2016
-
Mark
FN1-EGF gene fusions are recurrent in calcifying aponeurotic fibroma.
(
- Contribution to journal › Article
- 2015
-
Mark
Non-fibrosing sclerosing epithelioid fibrosarcoma: An unusual variant.
2015) In Histopathology(
- Contribution to journal › Letter
- 2014
-
Mark
Myoepithelioma of bone with a novel FUS-POU5F1 fusion gene
(
- Contribution to journal › Article
-
Mark
Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma.
(
- Contribution to journal › Article
- 2012
-
Mark
SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors.
(
- Contribution to journal › Article
- 2011
-
Mark
Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study
(
- Contribution to journal › Article
-
Mark
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
(
- Contribution to journal › Article
- 2010
-
Mark
Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma.
(
- Contribution to journal › Article