Evaluation of the Specificities of Five DNA Amplification Methods for the Detection of Neisseria gonorrhoeae
Author:
Affiliation:
1. Genitourinary Infections Reference Laboratory, Public Health Laboratory, Bristol Royal Infirmary, Bristol, BS2 8HW
2. Liverpool Public Health Laboratory, University Hospital at Aintree, Liverpool, L9 7AL, United Kingdom
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.41.2.835-837.2003
Reference22 articles.
1. Brunton, W. A. T., H. Young, and D. R. K. Fraser. 1980. Isolation of Neisseria lactamica from the female genital tract. Br. J. Vener. Dis.56:325-326.
2. Carrick, C. S., J. A. M. Fyfe, and J. K. Davies. 1998. Neisseria gonorrhoeae contains multiple copies of a gene that may encode a site-specific recombinase and is associated with DNA rearrangements. Gene220:21-29.
3. Relationship between plasmid content and auxotype in Neisseria gonorrhoeae isolates
4. Evaluation of AMPLICOR Neisseria gonorrhoeae PCR Using cppB Nested PCR and 16S rRNA PCR
5. Fiorito, S. M., P. G. Galarza, M. Sparo, E. I. Pagano, and C. I. Oviedo. 2001. An unusual transmission of Neisseria meningitidis.Sex. Transm. Dis.>28:29-32.
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