Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.11889/2018
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dc.contributor.authorEssawi, Tamer-
dc.contributor.authorAdwan, Kamel-
dc.contributor.authorAbu Hassan, Nael-
dc.contributor.authorAdwan, Ghaleb-
dc.contributor.authorSaleh, Ahmad-
dc.date.accessioned2016-10-08T06:45:02Z-
dc.date.available2016-10-08T06:45:02Z-
dc.date.issued2003-5-
dc.identifier.urihttp://hdl.handle.net/20.500.11889/2018-
dc.description.abstractThirty-five methicillin-resistant Staphylococcus aureus (MRSA) clinical isolates were collected from 3 hospitals in the northern and southern parts of Palestine between February and May 1998. These isolates were typed by ribosome spacer PCR (RSPCR) and arbitrarily primed PCR (AP-PCR). RS-PCR generated 9 different genotypes. The use of AP–PCR provided a high resolution typing method and allowed us to define 11 different clusters. Three major clusters, however, based on the combination of both typing methods, spread throughout the neonatal and intensive care units of Rafidya Hospital during the entire period.-
dc.language.isoenen_US
dc.publisherResearchGateen_US
dc.subject.lcshStaphylococcus aureus infections-
dc.subject.lcshPolymerase chain reaction-
dc.titleTyping of methicillin-resistant staphylococcus aureus by ribosome spacer and arbitrarily primed polymerase chain reactionen_US
dc.typeArticleen_US
newfileds.departmentClinical Laboratoryen_US
newfileds.item-access-typeopen_accessen_US
item.fulltextWith Fulltext-
item.languageiso639-1other-
item.grantfulltextopen-
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