Kangsadalampai, S., Fargesberth, A., Çağlayan, S.H., Board, P.G., “New Mutations Causing the Premature Termination of Translation in the a Subunit Gene of Coagulation Factor XIII”, Thrombosis and Haemostasis, 76, 2, 139-142, 1996. Dil Türkçe
Wright, J., Teraoka, S., Önengüt, S., Tolun, A., Gatti, R.A., Ochs, H.D., Concannon, P., “High Frequency of Distinct ATM Gene Mutations in Ataxia Telangiectasia”, American Journal of Human Genetics, 59, 4, 839-846, 1996. Dil Türkçe
Calafell, F., Underhill, P., Tolun, A., Angelicheva, D., Kalaydjieva, L., “From Asia to Europe: Mitochondrial DNA Sequence Variability in Bulgarians and Turks”, Annals of Human Genetics, 60, 35-49, 1996. Dil Türkçe
Altay, C., Gürgey, A., Başak, A.N., Tadmouri, G.O., Schroederkurt, T., “Fanconi Aplastic Anemia Associated with Beta Thalassemia Trait”, American Journal of Hematology, 52, 3, 239-240, 1996. Dil Türkçe
Kangsadalampai, S., Coggan, M., Çağlayan, S.H., Aktuğlu, G., Board, P.G., “Application of HUMF 13A01 (AAAG)(N) STR Polymorphism to the Genetic Diagnosis of Coagulation Factor XIII Deficiency”, Thrombosis and Haemostasis, 76, 6, 879-882, 1996. Dil Türkçe
Çağlayan, S.H., Gökmen, Y., Kırdar, B., “Polymorphisms Associated with the Fviii and Fix Genes in the Turkish population”, Haemophilia, 1, 3, 184-189, 1995. Dil Türkçe
Telatar, M., Lange, E., Uhrhammer, N., Gatti, R.A., “New Localization of Ncam, Proximal to Drd2 at Chromosome 11q23”, Mammalian Genome, 6, 1, 59-60, 1995. Dil Türkçe
Altay, C., Başak, A.N., “Molecular Basis and Prenatal Diagnosis of Hemoglobinopathies in Turkey”, International Journal of Pediatric Hematology/Oncology, 2, 4, 283-290, 1995. Dil Türkçe
Lange, E., Borresen, A.L., Tolun, A., et al., “Location of an Ataxia Telangiectasia Gene to an Simila to 500 kb Interval on Chromosome 11q23.1 Linkage Analysis of 176 Families by an International Consortium”, American Journal of Human Genetics, 57, 1, 112-119, 1995. Dil Türkçe
Kavaslar, G.N., Telatar, M., Serdaroğlu, P., Deymeer, F., Özdemir, C., Tolun, A., “Identification of a One Basepair Deletion in Exon 6 of the Dystrophin Gene”, Human Mutation, 6, 1, 85-86, 1995. Dil Türkçe