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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 15, 2020
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cellsJakob Hofvander, Vickie Y Jo, Christopher D M Fletcher, et al.
Genes, Chromosomes & Cancer|May 1, 2013
Frequent PLAG1 gene rearrangements in skin and soft tissue myoepithelioma with ductal differentiationCristina R Antonescu, Lei Zhang, Sung Yun Shao, et al.
Cancer Genetics and Cytogenetics|September 1, 2010
Deep fibrous histiocytoma with a clonal karyotypic alteration: molecular cytogenetic characterization of a t(16;17)(p13.3;q21.3)Daniela V Frau, Enrico Erdas, Paola Caria, et al.
The American Journal of Surgical Pathology|August 7, 2023
PEComa of the Adrenal Gland: A Clinicopathologic Series of 7 CasesCraig B Wakefield, Peter M Sadow, Jason L Hornick, et al.
The American Journal of Surgical Pathology|March 7, 2020
A Novel SS18-SSX Fusion-specific Antibody for the Diagnosis of Synovial SarcomaEsther Baranov, Matthew J McBride, Andrew M Bellizzi, et al.
The American Journal of Surgical Pathology|September 7, 2023
Infantile Sinonasal Myxoma Is Clinically and Genetically Distinct From Other Myxomas of the Craniofacial Bones and From Desmoid FibromatosisIgor Odintsov, Fei Dong, Jeffrey P Guenette, et al.
The American Journal of Surgical Pathology|May 29, 2019
Cutaneous Syncytial Myoepithelioma Is Characterized by Recurrent EWSR1-PBX3 FusionsVickie Y Jo, Cristina R Antonescu, Brendan C Dickson, et al.
The American Journal of Surgical Pathology|December 20, 2023
Melanotic PEComa: A Rare But Distinctive Subtype Analyzed in a Series of 7 CasesArnaud de la Fouchardiere, David J Papke, Daniel Pissaloux, et al.
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