Toplantı Özeti

​​​Akdoğan, Z., Güven, B.​​​​​, “Hidrolojik Modellemede Parametrik Duyarlılığının Değerlendirilmesi İstanbul İli Örneği”​​​​​, 3. Ulusal Çevre Kongresi​​​​​, 2016, Marmaris, Türkiye​​​​​, 3. Ulusal Çevre Kongresi Özet Kitabı​​​​, 1​​​​​, 69​​​​​, 2016.​​​​ ​​

Türkçe

Gökcümen, Ö., Alkan, C., Kavak, P., Somel, M., Uğurlu, S., Dal, E., Bugra-Bilge, K., Güngör, T., Şahinalp, C., Özören, N., Bekpen, C., 'Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa', American Journal of Physical Anthropology, 153, 126-127, 2014.

Türkçe

Akan P, Bekbolet M, “Adsorption of Molecular Size Fracations of Humic Acid onto Anion Doped TiO2 Specimens”, Second International Conference on Recycling and Reuse, 2014, İstanbul/Türkiye, Second International Conference on Recycling and Reuse Book of Abstracts, 2014.

Türkçe

Weckhuysen, S., Suls, A., Djemie, T., Sterbova, K., Hoffman-Zacharska, D., Talvik, T., Çağlayan, H. et al. 'Trio Exome Sequencing in 31 Patients with SCN1A Negative Dravet Syndrome Leads to the Detection of Another Recessive SCN1B Mutation and the Discovery of at Least Two Novel Epilepsy Genes', Epilepsia, 55, 2, 81-81 Meeting Abstract: p239, 2014.

Türkçe

Suls, A., Jaehn, J.J., Kecskes, A., Weber, Y., Weckhuysen, S., Craiu, D.C., Siekierska, A., Djemie, T., Afrikanova, T., Gormley, P., von Spiczak, S., Kluger, G., Iliescu, C.M., Talvik, T., Talvik, I., Meral, C., Çağlayan, S.H. et al. 'De Novo Loss-of-Function Mutations in CHD2 Cause A Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features With Dravet Syndrome', Epilepsia, 55, 2, 79-80, Meeting Abstract: p239, 2014.

Türkçe

Altındağ, E., Gündoğdu, A., Usluer, S., Çağlayan, H., Baykara, B., 'Down syndrome and late onset myoclonic epilepsy in Down syndrome: investigation of EPM1 gene mutations in two cases', Journal of Neurology,  Meeting Abstract: PP2050, 261, S328-S328, 2014.

Türkçe

Altındağ, E., Gündoğdu, A., Usluer, S., Çağlayan, H., Baykan, B., 'Down syndrome and late onset myoclonic epilepsy in Down syndrome: investigation of EPM1 gene mutations in two casesP.M., Başak, A.N., 'C9orf72 hexanucleotide repeat expansion in Turkish ALS patients', European Journal of Neurology,  Meeting Abstract: PP2050, 21, 496-496, 2014.

Türkçe

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