Publications by authors named "Cihan Oner"

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The molecular basis of familial hypercholesterolaemia in Turkish patients.
M Mert Sözen, Ros Whittall, Cihan Oner, Ayşegül Tokatli, H Serap Kalkanoğlu, Reyhan Oner

Atherosclerosis· May 2005

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Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
Stephan M Tanner, Zhongyuan Li, James D Perko, Cihan Oner, Mualla Cetin

Proc Natl Acad Sci U S A· March 2005

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Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosa.
Riza Köksal Ozgül, Hakan Durukan, Ayse Turan, Cihan Oner, Ay Ogüs

Hum Mutat· May 2004

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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 Middle East.
Stephan M Tanner, Zhongyuan Li, Ryan Bisson, Ceren Acar, Cihan Oner, Reyhan Oner

Hum Mutat· April 2004

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

J Genet· April 2004

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

Eur J Haematol· July 2003

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Effects of neutral, cationic, and anionic chromium ascorbate complexes on isolated human mitochondrial and genomic DNA.
Ahmet Nedim Ay, Birgül Zümreoglu-Karan, Reyhan Oner, Canan Unaleroglu, Cihan Oner

J Biochem Mol Biol· July 2003

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Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion.
Esra Birben, Reyhan Oner, Cihan Oner, Fatma Gümrük, Ciğdem Altay

Br J Haematol· July 2002

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