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Clinical Validation of the Abbott RealTime High Risk HPV Assay According to the Guidelines for Human Papillomavirus DNA Test Requirements for Cervical Screening

This study showed that the Abbott RealTime High Risk HPV assay fulfilled cross-sectional clinical equivalence and reproducibility criteria of international consensus guidelines, which indicates that this assay can be considered clinically validated for cervical cancer screening purposes.

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Detaylı Bibliyografya
Asıl Yazarlar: Hesselink, A. T., Meijer, C. J. L. M., Poljak, M., Berkhof, J., van Kemenade, F. J., van der Salm, M. L., Bogaarts, M., Snijders, P. J. F., Heideman, D. A. M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Microbiology 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3697677/
https://ncbi.nlm.nih.gov/pubmed/23637297
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JCM.00633-13
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