SCI

Uyan, Ö., Ömür, Ö., Ağım, Z.S., Özoğuz, A., Li, H., Parman, Y., Deymeer, F., Oflazer, P., Koç, F., Tan, E., Özçelik, H., Başak, A.N., “Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor”, PLoS One, 8, 8, Article Number: e72381, 2013.

Türkçe

Taşcı Marangoz, N., Yüzbaşıoğlu, İ,S, Çelen, Z., Ekim, T., Bilgin, A.N., “Molecular phylogeny of Galanthus (Amaryllidaceae) of Anatolia inferred from multiple nuclear and chloroplast DNA regions”, Turkish Journal of Botany, 37, 6, 993-1007, 2013.

Türkçe

Suls, A., Jaehn, J.A., Kecskes, A., Çağlayan, S.A. et al, “De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome”, American Journal of Human Genetics, 93, 5, 967-975, 2013.

Türkçe

Sayfalar