MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever von ÇAKIR, Necati, AZAKLI, Hülya, ÜSTEK, Duran, UYSAL, Ömer, GÖZKE, Eren

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Terminal osseous dysplasia with pigmentary defects (TODPD) in a Turkish girl with new skin findings von Azakli, Hülya, Akkaya, Ayse Deniz, Aygün, Murat Serhat, Demirkesen, Cüyan, Eraslan, Serpil, Kayserili, Hülya

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Expanding the spectrum of syndromic PPP2R3C‐related XY gonadal dysgenesis to XX gonadal dysgenesis von Altunoglu, Umut, Börklü, Esra, Shukla, Anju, Escande‐Beillard, Nathalie, Ledig, Susanne, Azaklı, Hülya, Nayak, Shalini S., Eraslan, Serpil, Girisha, Katta Mohan, Kennerknecht, Ingo, Kayserili, Hülya

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Origin and spread of human mitochondrial DNA haplogroup U7 von Sahakyan, Hovhannes, Hooshiar Kashani, Baharak, Tamang, Rakesh, Kushniarevich, Alena, Francis, Amirtharaj, Costa, Marta D., Pathak, Ajai Kumar, Khachatryan, Zaruhi, Sharma, Indu, van Oven, Mannis, Parik, Jüri, Hovhannisyan, Hrant, Metspalu, Ene, Pennarun, Erwan, Karmin, Monika, Tamm, Erika, Tambets, Kristiina, Bahmanimehr, Ardeshir, Reisberg, Tuuli, Reidla, Maere, Achilli, Alessandro, Olivieri, Anna, Gandini, Francesca, Perego, Ugo A., Al-Zahery, Nadia, Houshmand, Massoud, Sanati, Mohammad Hossein, Soares, Pedro, Rai, Ekta, Šarac, Jelena, Šarić, Tena, Sharma, Varun, Pereira, Luisa, Fernandes, Veronica, Černý, Viktor, Farjadian, Shirin, Singh, Deepankar Pratap, Azakli, Hülya, Üstek, Duran, Ekomasova Trofimova, Natalia, Kutuev, Ildus, Litvinov, Sergei, Bermisheva, Marina, Khusnutdinova, Elza K., Rai, Niraj, Singh, Manvendra, Singh, Vijay Kumar, Reddy, Alla G., Tolk, Helle-Viivi, Cvjetan, Svjetlana, Lauc, Lovorka Barac, Rudan, Pavao, Michalodimitrakis, Emmanuel N., Anagnou, Nicholas P., Pappa, Kalliopi I., Golubenko, Maria V., Orekhov, Vladimir, Borinskaya, Svetlana A., Kaldma, Katrin, Schauer, Monica A., Simionescu, Maya, Gusar, Vladislava, Grechanina, Elena, Govindaraj, Periyasamy, Voevoda, Mikhail, Damba, Larissa, Sharma, Swarkar, Singh, Lalji, Semino, Ornella, Behar, Doron M, Yepiskoposyan, Levon, Richards, Martin B., Metspalu, Mait, Kivisild, Toomas, Thangaraj, Kumarasamy, Endicott, Phillip, Chaubey, Gyaneshwer, Torroni, Antonio, Villems, Richard

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A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology von Ustek, Duran, Sirma, Sema, Gumus, Ergun, Arikan, Muzaffer, Cakiris, Aris, Abaci, Neslihan, Mathew, Jaicy, Emrence, Zeliha, Azakli, Hulya, Cosan, Fulya, Cakar, Atilla, Parlak, Mahmut, Kursun, Olcay

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Il Özel Idarelerinde Yeniden Yapilan(ama)ma Çabalari ve Uygulamada Karsilasilan Sorunlar/(In)Capability of Re-Organization Efforts and Implementation Problems in The Special Provin... von Azakli, Sedat, Tek, Hülya

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Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease von Remmers, Elaine F, Cosan, Fulya, Kirino, Yohei, Ombrello, Michael J, Abaci, Neslihan, Satorius, Colleen, Le, Julie M, Yang, Barbara, Korman, Benjamin D, Cakiris, Aris, Aglar, Oznur, Emrence, Zeliha, Azakli, Hulya, Ustek, Duran, Tugal-Tutkun, Ilknur, Akman-Demir, Gulsen, Chen, Wei, Amos, Christopher I, Dizon, Michael B, Kose, Afet Akdag, Azizlerli, Gulsevim, Erer, Burak, Brand, Oliver J, Kaklamani, Virginia G, Kaklamanis, Phaedon, Ben-Chetrit, Eldad, Stanford, Miles, Fortune, Farida, Ghabra, Marwen, Ollier, William E R, Cho, Young-Hun, Bang, Dongsik, O'Shea, John, Wallace, Graham R, Gadina, Massimo, Kastner, Daniel L, Gül, Ahmet

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Mitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosis von Gurses, Candan, Azakli, Hulya, Alptekin, Ahmet, Cakiris, Aris, Abaci, Neslihan, Arikan, Muzaffer, Kursun, Olcay, Gokyigit, Aysen, Ustek, Duran

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Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: A case of mesial temporal lobe epilepsy with hippocampal scl... von Azakli, Hulya, Gurses, Candan, Arikan, Muzaffer, Aydoseli, Aydın, Aras, Yavuz, Sencer, Altay, Gokyigit, Aysen, Bilgic, Bilge, Ustek, Duran

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The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still’s disease von Cosan, Fulya, Emrence, Zeliha, Erbag, Gokhan, Azakli, Hulya, Yilmazer, Baris, Yazici, Ayten, Ekmekci, Sema Sirma, Abaci, Neslihan, Ustek, Duran, Cefle, Ayse

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Hypoxia Induces Erythropoietin Receptor Expression on K562 Cell Line von Abaci, Neslihan, Cosan, Fulya, Gulec, Cagri, Azakli, Hulya, Emrence, Zeliha, Sirma-Ekmekci, Sema, Cakiris, Aris, Oku, Basar, Ustek, Duran

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İl Özel İdarelerinde Yeniden Yapılan(Ama)Ma Çabaları Ve Uygulamada Karşılaşılan Sorunlar von AZAKLI, Sedat, TEK, Hülya

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Tribological and mechanical properties of Al alloyed bearings von Unlue, Bekir Sadik, Durmus, Huelya, Akguen, Selda

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Kamu Yönetiminde Yenilikçi Bir Yaklaşım ve Dönüşüm Modeli: Yatırım İzleme ve Koordinasyon Başkanlığı von Tamer, Mehmet, Dönmez, Demet

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Contents von Dergisi, Oneri

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İÇİNDEKİLER

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İÇİNDEKİLER

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Kamu yönetiminde yenilikçi bir yaklaşım ve dönüşüm modeli: Yatırım İzleme ve Koordinasyon Başkanlığı von Tamer,Mehmet, Dönmez,Demet

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