Fen-Edebiyat Fakültesi

Turanlı, E.T., Karacan, I., Esatlıoğlu, S. N., ŞahIn, S., Kasapcopur, O., Tolun, A., Seyahi, E., “Whole Genome Linkage and Exome Sequencing Analyses in Takayasu Arteritis Familirs”, Annals of the Rheumatic Diseases, 77, 231-232, 2018.

Türkçe

Solmaz, B., Özyurt, M.G., Ata, D.B., Akçimen, F., Shabsog, M., Türker, K.S., Alçık, H., AlgIn, O., Başak, A.N., Özgür, M., Çavdar, S., “Assessment of the CorticospInal Fiber Integrity in Mirror Movement Disorder“, Journal of ClInical Neuroscience, 54, 69-76, 2018.

Türkçe

Shabbir, R.M.K., Nalbant, G., Ahmad, N., Malik, S., Tolun, A., “Homozygous CHST11 Mutation in Chondrodysplasia, Brachydactyly, Overriding Digits, ClIno-symphalangism and Synpolydactyly“, Journal of Medical Genetics, 55, 7, 489-496, 2018.

Türkçe

Parman, Y., Durmuş, H., Candayan, A., Akçay, H.İ., Yunisova, G., Ulukan, Ç., Serdaroğlu, P., Deymeer, F., Battaloğlu, E., “ClInical and Genetic Features in X-Linked Charcot-Marie-Tooth Neuropathy (Cmt-X) Patients from Turkey“, Neurology, 90, 2018.

Türkçe

Mitropoulos, K., Papadima, E.M., Xeromerisiou, G., Balasopoulou, A., Başak, A.N., et al., “Genomic Variants in The Fto Gene Are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients“, Publıc Health Genomıcs, 21, 17-17, 2018.

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