Comparison study of mecA gene-based pcr with phenotypic methods for detecting biofilm forming methicillin resistant staphylococcus aureus isolates and comparison of mecA with femA, femB, and mecC genes
Other Title(s)
دارسة مقارنة تفاعل البلمرة المتسلسل المعتمد على الجين mecA مع الطرق المظهرية للكشف عن مقاومة الميثيسيلين في عزلات المكورات العنقودية المكونة للغشاء الحيوي و مقارنة جين mecA مع جينات A ، femB و mecC
Joint Authors
Turki, Ahmad Muhammad
Barzani, Khadijah Khalil
Abd, Janan Jamil
Source
Journal of University of Anbar for Pure Science
Issue
Vol. 11, Issue 1 (30 Apr. 2017), pp.1-8, 8 p.
Publisher
University of Anbar College of Science
Publication Date
2017-04-30
Country of Publication
Iraq
No. of Pages
8
Main Subjects
American Psychological Association (APA)
Barzani, Khadijah Khalil& Turki, Ahmad Muhammad& Abd, Janan Jamil. 2017. Comparison study of mecA gene-based pcr with phenotypic methods for detecting biofilm forming methicillin resistant staphylococcus aureus isolates and comparison of mecA with femA, femB, and mecC genes. Journal of University of Anbar for Pure Science،Vol. 11, no. 1, pp.1-8.
https://search.emarefa.net/detail/BIM-841890
Modern Language Association (MLA)
Barzani, Khadijah Khalil…[et al.]. Comparison study of mecA gene-based pcr with phenotypic methods for detecting biofilm forming methicillin resistant staphylococcus aureus isolates and comparison of mecA with femA, femB, and mecC genes. Journal of University of Anbar for Pure Science Vol. 11, no. 1 (2017), pp.1-8.
https://search.emarefa.net/detail/BIM-841890
American Medical Association (AMA)
Barzani, Khadijah Khalil& Turki, Ahmad Muhammad& Abd, Janan Jamil. Comparison study of mecA gene-based pcr with phenotypic methods for detecting biofilm forming methicillin resistant staphylococcus aureus isolates and comparison of mecA with femA, femB, and mecC genes. Journal of University of Anbar for Pure Science. 2017. Vol. 11, no. 1, pp.1-8.
https://search.emarefa.net/detail/BIM-841890
Data Type
Journal Articles
Language
English
Record ID
BIM-841890
