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Detection of Bartonella henselae and Bartonella quintana by a simple and rapid procedure using broad-range PCR amplification and direct single-strand.

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Presentation on theme: "Detection of Bartonella henselae and Bartonella quintana by a simple and rapid procedure using broad-range PCR amplification and direct single-strand."— Presentation transcript:

1 Detection of Bartonella henselae and Bartonella quintana by a simple and rapid procedure using broad-range PCR amplification and direct single-strand sequencing of part of the 16S rRNA gene  Daniel Goldenberger, Tobias Schmidheini, Martin Altwegg  Clinical Microbiology and Infection  Volume 3, Issue 2, Pages (April 1997) DOI: /j tb00604.x Copyright © 1997 European Society of Clinical Infectious Diseases Terms and Conditions

2 Figure 1 Alignment of partial 16S rRNA gene sequences of B. henselae. Gaps introduced for optimal alignment are represented by a dot. Variable nucleotides are in bold. Clinical Microbiology and Infection 1997 3, DOI: ( /j tb00604.x) Copyright © 1997 European Society of Clinical Infectious Diseases Terms and Conditions


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