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Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study

Chordomas are rare embryogenetic tumors, arising from remnants of the notochord, characterized by local invasiveness and variable tendency for recurrence. No molecular markers are currently used in a clinical setting to distinguish chordomas with an indolent or an aggressive pattern. Among the genet...

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Detaylı Bibliyografya
Asıl Yazarlar: Longoni, Mauro, Orzan, Francesca, Stroppi, Michela, Boari, Nicola, Mortini, Pietro, Riva, Paola
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Duke University Press 2008
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2600838/
https://ncbi.nlm.nih.gov/pubmed/18094369
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1215/15228517-2007-048
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