Moleküler Biyoloji ve Genetik

Van Rheenen, W., Pulit, S.L., Dekker, A.M., Kavak, E., Başak, A.N., “Project MInE: Study Design and Pilot Analyses of a Large-scale Whole-genome Sequencing Study in Amyotrophic Lateral Sclerosis“, European Journal of Human Genetics, 26, 10, 1537-1546, 2018.

Türkçe

Türkgenç, B., Şanlıdağ, B., Eker, A., Giray, A., Kütük, O., Yakıcıer, C., Tolun, A., Temel, S.G., “STUB1 Polyadenylation Signal Variant ACAAA does not Affect Polyadenylation but Decreases STUB1 Translation Causing SCAR16“, Human Mutation, 39, 10, 1344-1348, 2018.

Türkçe

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

Sayfalar