Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Artigo
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish FamilyDursun, Fatma ; Mohamoud, Hussein Sheikh Ali ; Karim, Noreen ; Naeem, Muhammad ; Jelani, Musharraf ; Kırmızıbekmez, HevesJournal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.472-477 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Characterization of class 1 and class 2 integron gene cassettes in Escherichia coli strains isolated from urine cultures: a multicenter studyÇopur Çiçek, Ayşegül ; Sandallı, Cemal ; Budak, Emine Esra ; Yağmur, Gülhan ; Çizmeci, Zeynep ; Ak, Sibel ; Balcı, Pervin Özlem ; Şay Coşkun, Safiye Umut ; Ay Altıntop, Yasemin ; Fırat, Mehmet ; Sarı, Fatma ; Çalışkan, Ahmet ; Yıldız, Nazan ; Sancaktar, Metin ; Özgümüş, Osman BirolMikrobiyoloji bülteni, 2016-04, Vol.50 (2), p.175-185 [Periódico revisado por pares]TurkeyTexto completo disponível |
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3 |
Material Type: Artigo
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Heterogeneous macrolide resistance in methicillin-resistant Staphylococcus aureus isolates: investigation of resistance mechanisms and clonalityHoşbul, Tuğrul ; Bozdoğan, Bülent ; Haznedaroğlu, Tunçer ; Ozyurt, MustafaMikrobiyoloji bülteni, 2013-04, Vol.47 (2), p.211-222 [Periódico revisado por pares]TurkeyTexto completo disponível |
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4 |
Material Type: Artigo
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Determination of hepatitis B virus genotypes by DNA sequence analysis in patients from Ankara, TurkeyKülah, Canan ; Cirak, Meltem YalinayMikrobiyoloji bülteni, 2010-04, Vol.44 (2), p.245 [Periódico revisado por pares]TurkeySem texto completo |
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5 |
Material Type: Artigo
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A novel Salmonella Typhimurium plasmid, pAnkS: an example for plasmid evolution in antibiotic resistanceSahin, Fikret ; Karasartova, Djursun ; Gerçeker, Devran ; Aysev, A Derya ; Erdem, BirselMikrobiyoloji bülteni, 2008-07, Vol.42 (3), p.383 [Periódico revisado por pares]TurkeySem texto completo |
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6 |
Material Type: Artigo
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Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)Çelmeli, Gamze ; Türkkahraman, Doğa ; Çürek, Yusuf ; Houghton, Jayne ; Akçurin, Sema ; Bircan, İffet Darendeliler,Fatma FeyzaJournal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.80-84 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |