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Güven, A., Tolun, A., “TBC1D24 truncating mutation resulting in severe neurodegeneration”, Journal of Medical Genetics, 50, 3, 199-202, 2013. Dil Türkçe
Gökçe, M., Gümrük, F., Haliloğlu, G., Serdaroğlu, E., Çağlayan, H., “Double trouble: Duchenne muscular dystrophy and hemophilia”, Pediatric Blood & Cancer, 60, 3, 525-525, 2013. Dil Türkçe
Fuss, S.H., Zhu, Y., Mombaerts, P., “Odorant receptor gene choice and axonal wiring in mice with deletion mutations in the odorant receptor gene SR1”, Molecular and Cellular Neuroscience”, 56, 212-224, 2013. Dil Türkçe
Berber, E., Pehlevan, F., Akın, M., Çapan, Ö.Y., Kavaklı, K., Çağlayan, S.H., “A Common VWF Exon 28 Haplotype in the Turkish Population”, Clinical and Applied Thrombosis-Hemostasis, 19, 5, 550-556, 2013. Dil Türkçe
Bakış, Y., Otu, H. H., Taşçı, N., Meydan, C., Bilgin, N., Yüzbaşıoğlu, S., Sezerman, O. U., “Testing robustness of relative complexity measure method constructing robust phylogenetic trees for Galanthus L. Using the relative complexity measure”, BMC Bioinformatics, 14, Article Number: 20, 2013. Dil Türkçe
Arslan, M., Yis, U., Çağlayan, H., Akın, R., “A novel mutation in the sodium channel alpha 1 subunit gene in a child with Dravet syndrome in Turkey”, Neural Regeneration Research, 8, 10, 955-958, 2013. Dil Türkçe
Agim, Z.S., Esendal, M., Briollais, L., Uyan, Ö., Meschian, M., Martinez, L.A.M., Ding, Y.M., Başak, A.N., Özcçlik, H., “Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia”, PLoS One, 8, 1, Article Number: e53042, 2013. Dil Türkçe
Şahin, H. B., Çelik, A., “Drosophila Eye Development and Photoreceptor Specification”, 2013. Dil Türkçe
Parman, Y., Battaloğlu, E., “Recessively transmitted predominantly motor neuropathies”, Peripheral Nerve Disorders, Book Series: Handbook of Clinical Neurology, Said G, Krarup C (Derleyenler), 115, 847-861, Elsevier, 2013. Dil Türkçe
