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

Get full text

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

Get full text

Expanding the spectrum of syndromic PPP2R3C‐related XY gonadal dysgenesis to XX gonadal dysgenesis by 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

Get full text

Origin and spread of human mitochondrial DNA haplogroup U7 by 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

Get full text

A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology by 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

Get full text

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

Get full text

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... by Azakli, Hulya, Gurses, Candan, Arikan, Muzaffer, Aydoseli, Aydın, Aras, Yavuz, Sencer, Altay, Gokyigit, Aysen, Bilgic, Bilge, Ustek, Duran

Get full text

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

Get full text

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

Get full text

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... by Azakli, Sedat, Tek, Hülya

Get full text