[1] Unemo M, Olcen P, Albert J, et al. Comparison of serologic and genetic porB-based typing of Neisseria gonorrhoeae: consequences for future characterization. J Clin Microbiol. 2003 Sep;41(9):4141-7. [2] Van Looveren M, Ison CA, Ieven M, et al. Evaluation of the discriminatory power of typing methods for Neisseria gonorrhoeae. J Clin Microbiol 1999; 37:2183-2188. [3] O'Rourke M, Ison CA, Renton AM, et al. Opa-typing: a high-resolution tool for studying the epidemiology of gonorrhoea. Mol Microbiol 1995; 17:865-875. [4] Viscidi RP,Demma JC, Gu J, et al. Comparison of sequencing of the por gene and typing of the opa gene for discrimination of Neisseria gonorrhoeae strains from sexual contacts. J Clin Microbiol 2000; 38:4430-4438. [5] BJ?RN-ARNE LINDSTEDT, EVEN HEIR,TRAUTE VARDUND, et al. Comparative Fingerprinting Analysis of Campylobacter jejuni subsp. jejuni Strains by Amplified-Fragment Length Polymorphism Genotyping. J Clin Microbiol, 2000:38:3379–3387 [6] ZHI-YUAN SHI, PETER YUK-FONG LIU, YEU-JUN LAU, et al. Epidemiological Typing of Isolates from an Outbreak of Infection with Multidrug-Resistant Enterobacter cloacae by Repetitive Extragenic Palindromic Unit b1-Primed PCR and Pulsed-Field Gel Electrophoresis. J Clin Microbiol, 1996:34:2784–2790. [7] Ma°rten Kivi,Ylva Tindberg, Mikael So¨rberg,et al. Concordance of Helicobacter pylori Strains within Families. J Clin Microbiol,2003:41: 5604–5608 [8] S. H. GILLESPIE,A. DICKENS, T. D. MCHUGH. False Molecular Clusters due to Nonrandom Association of IS6110 with Mycobacterium tuberculosis. J Clin Microbiol,2000:38:2081–2086. [9] JAVIER GARAIZAR, NURIA LO′PEZ-MOLINA, IDOIA LACONCHA, et al. Suitability of PCR Fingerprinting, Infrequent-Restriction-Site PCR, and Pulsed-Field Gel Electrophoresis, Combined with Computerized Gel Analysis, in Library Typing of Salmonella enterica Serovar Enteritidis. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000:66: 5273–5281. |