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The Journal of Pathology
|
February 10, 2009
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions
Karolin H Hallor, Raf Sciot, Johan Staaf, et al.
The Journal of Pathology
|
December 21, 2010
The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target
Asem Shalaby, Nadège Presneau, Hongtao Ye, et al.
The American Journal of Surgical Pathology
|
December 21, 2018
PRDM10-rearranged Soft Tissue Tumor: A Clinicopathologic Study of 9 Cases
Florian Puls, Nischalan Pillay, Henrik Fagman, et al.
Nature Genetics
|
October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordoma
Nischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.
The Journal of Pathology
|
December 21, 2010
Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study
Nadège Presneau, Asem Shalaby, Hongtao Ye, et al.
Nature Genetics
|
November 8, 2011
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
Twinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.
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of 5
Search research articles
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Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
The Journal of Pathology
|
February 10, 2009
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions
Karolin H Hallor, Raf Sciot, Johan Staaf, et al.
The Journal of Pathology
|
December 21, 2010
The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target
Asem Shalaby, Nadège Presneau, Hongtao Ye, et al.
The American Journal of Surgical Pathology
|
December 21, 2018
PRDM10-rearranged Soft Tissue Tumor: A Clinicopathologic Study of 9 Cases
Florian Puls, Nischalan Pillay, Henrik Fagman, et al.
Nature Genetics
|
October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordoma
Nischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.
The Journal of Pathology
|
December 21, 2010
Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study
Nadège Presneau, Asem Shalaby, Hongtao Ye, et al.
Nature Genetics
|
November 8, 2011
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
Twinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.
Page
of 5