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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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Библиографические подробности
Главные авторы: 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.
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Microbiology 2013
Предметы:
Online-ссылка: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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