Hereditary Juvenile Cobalamin Deficiency Caused by Mutations in the Intrinsic Factor Gene von Tanner, Stephan M., Li, Zhongyuan, Perko, James D., Öner, Cihan, Çetin, Mualla, Altay, Çiğdem, Yurtsever, Zekiye, David, Karen L., Faivre, Laurence, Ismail, Essam A., Gräsbeck, Ralph, de la Chapelle, Albert

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Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the... von Tanner, Stephan M., Li, Zhongyuan, Bisson, Ryan, Acar, Ceren, Öner, Cihan, Öner, Reyhan, Çetin, Mualla, Abdelaal, Mohamed A., Ismail, Essam A., Lissens, Willy, Krahe, Ralf, Broch, Harald, Gräsbeck, Ralph, Chapelle, Albert de la

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The molecular basis of familial hypercholesterolaemia in Turkish patients von Sözen, M. Mert, Whittall, Ros, Öner, Cihan, Tokatlı, Ayşegül, Kalkanoğlu, H. Serap, Dursun, Ali, Coşkun, Turgay, Öner, Reyhan, Humphries, Steve E.

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Deep Levels in n-Type 4H-Silicon Carbide Epitaxial Layers Investigated by Deep-Level Transient Spectroscopy and Isochronal Annealing Studies von Mannan, Mohammad A., Nguyen, Khai V., Pak, Rahmi O., Oner, Cihan, Mandal, Krishna C.

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A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity von MERGEN, Mehmet, MERGEN, Hatice, OZATA, Metin, ONER, Reyhan, ONER, Cihan

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Mitochondrial DNA sequence variation in the Anatolian Peninsula (Turkey) von Mergen, Hatice, Oner, Reyhan, Oner, Cihan

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Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion von Birben, Esra, Öner, Reyhan, Öner, Cihan, Gümrük, Fatma, Altay, Çiğdem, Gürgey, Aytemiz

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Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosa von Özgü, Rıza Köksal, Durukan, Hakan, Turan, Ayşe, Öner, Cihan, Öğüş, Ay, Farber, Debora B.

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Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients von Birben, Esra, Öner, Cihan, Öner, Reyhan, Altay, Çigˇdem, Gürgey, Aytemiz

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RAPID COMMUNICATION: A Novel Melanocortin 4 Receptor (MC4R) Gene Mutation Associated with Morbid Obesity von Mergen, Mehmet, Mergen, Hatice, Ozata, Metin, Oner, Reyhan, Oner, Cihan

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Vitamin d-receptor gene polymorphisms and vertebral bone density in men with idiopathic hypogonadotrophic hypogonadism von Ozisik, G, Mergen, H, Ozata, M, Uyanik, C, Caglayan, S, Turan, M, Bolu, E, Ilgin, S, Oner, R, Ozdemir, I C, Oner, C

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Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family von Sözen, M., Karaaslan, Ç., Öner, R., Gümrük, F., Özdemir, M.A., Altay, C., Gürgey, A., Öner, C.

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Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosa: MUTATIONS IN BRIEF von Özgü, Rıza Köksal, Durukan, Hakan, Turan, Ayşe, Öner, Cihan, Öğüş, Ay, Farber, Debora B.

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Molecular, Genetic and Epidemiologic Studies on Selective Complete C1q Deficiency in Turkey von Berkel, Ahmet Izzet, Birben, Esra, Öner, Cihan, Öner, Reyhan, Loos, Michael, Petry, Franz

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Genetically heterogeneous selective intestinal malabsorption of vitamin B 12 : Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and t... von Tanner, Stephan M., Li, Zhongyuan, Bisson, Ryan, Acar, Ceren, Öner, Cihan, Öner, Reyhan, Çetin, Mualla, Abdelaal, Mohamed A., Ismail, Essam A., Lissens, Willy, Krahe, Ralf, Broch, Harald, Gräsbeck, Ralph, Chapelle, Albert de la

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HOMOZYGOSITY FOR Hb E-SASKATOON [β22(B4)Glu → Lys] IN A TURKISH PATIENT von Birben, Esra, Öner, Reyhan, Öner, Cihan, Gümrük, Fatma, Gürgey, Aytemiz, Altay, Çigdem

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Investigation of ascorbate-Cu (II) induced cleavage of DNA by scanning tunneling microscopy von Zareie, M.Hadi, Erdem, Günhan, Öner, Cihan, Öner, Reyhan, Öǧüş, Ay, Pişkin, Erhan

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SEVERE β THALASSEMIA IN FRAMESHIFT CODON 6 (-A) HOMOZYGOTES: EFFECTS OF HAPLOTYPE ON PHENOTYPE von Birben, Esra, Öner, Cihan, Öner, Reyhan, Mergen, Hatice, Yesilipek, Akif, Gümrük, Fatma, Gürgey, Aytemiz, Altay, Çigdem

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The relative levels of α2-, α1-, and ζ-mRNA in HB H patients with different deletional and nondeletional α-thalassemia determinants von Smetanina, Natalia S., Öner, Cihan, Baysal, Erol, Öner, Reyhan, Bozkurt, Gülsen, Altay, Çigdem, Gürgey, Aytemiz, Adekile, Adekunle D., Gu, Li-Hao, Huisman, Titus H.J.

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Analysis of chimerism by PCR using mutant‐specific primers and sequencing of B‐gene region after allogenic bone marrow transplantation in sickle cell anemia von Gürgey, Aytemiz, Mesci, Lutfiye, Özerkam, Korkut, Öner, Cihan

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