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Laboratory Investigation; a Journal of Technical Methods and Pathology|January 11, 2005
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion geneFredrik Mertens, Christopher D M Fletcher, Cristina R Antonescu, et al.
The American Journal of Pathology|July 17, 2012
Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumorsSamuel Gebre-Medhin, Karolin H Nord, Emely Möller, et al.
The Journal of Pathology|January 17, 2002
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study GroupGiovanni Tallini, Howard Dorfman, Peter Brys, et al.
Ebiomedicine|October 14, 2023
Transcriptomic subtyping of malignant peripheral nerve sheath tumours highlights immune signatures, genomic profiles, patient survival and therapeutic targetsMaren Høland, Kaja C G Berg, Ina A Eilertsen, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 18, 2010
Genomic changes in chromosomes 10, 16, and X in malignant peripheral nerve sheath tumors identify a high-risk patient groupHelge R Brekke, Franclim R Ribeiro, Matthias Kolberg, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 2, 2009
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumorsKarolin H Hallor, Johan Staaf, Judith V M G Bovée, et al.
Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 27, 2013
TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewalPatrick J Killela, Zachary J Reitman, Yuchen Jiao, et al.
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