Usluer, S., Berber, E., Çağlayan, S., Pekçelen, Y., Ünüvar, A., “Establishment of High Resolution Melting Analysis for VWF Gene Mutation Scanning in Turkish Patients”, Haemophilia, 14, 2, 70-70, 2008. Dil Türkçe
Duru, N.S., Çelkan, T., Çivilibal, M., Özbek, N.O., Başak, A.N., Elevli, M., “Coinheritance of Sickle Cell Anemia and Hereditary Spherocytosis”, Pediatric Blood & Cancer, 51, 4, 560-563, 2008. Dil Türkçe
Shugaiv, E., Senergin, B., Battaloğlu, E., Serdaroğlu, P., Deymeer, F., Akalın, M.A., Parman, Y., “Clinicopathological and Genetic Study of CMT2”, Neuromuscular Disorders, 18, 9-10, 733-733, 2008. Dil Türkçe
Usluer, S., Berber, E., Çağlayan, S.H., Pekçelen, Y., Aksu, S., “Autosomal Dominant Inheritance of FXI Deficiency in Two Turkish Patients”, Haemophilia, 14, 110-110, 2008. Dil Türkçe
Etlik, O., Köksal, V., Arıcan-Barış, S.T., Barış, İ., “An Improved Tetra-Primer PCR Approach for the Detection of the FGFR3 G380R Mutation Responsible for Achondroplasia”, Molecular and Cellular Probes, 22, 2, 71-75, 2008. Dil Türkçe
Uğur, S.A., Tolun, A., “A Deletion in DRCTNNB1A Associated with Hypomyelination and Juvenile Onset Cataract”, European Journal of Human Genetics, 16, 2, 261-264, 2008. Dil Türkçe
Parman, Y., Çiftçi, F., Poyraz, M., Halefoğlu, A.M., Öge, A.E., Eraksoy, M., Saruhan-Direskeneli, G., Deymeer, F., Battaloğlu, E., “X Linked Charcot Marie Tooth Disease and Multiple Sclerosis”, Journal of Neurology, 254, 7, 953-955, 2007. Dil Türkçe
Yüksel, S., Hansen, J.N., “Transfer of Nisin Gene Cluster from Lactococcus Lactis ATCC 11454 into the Chromosome of Bacillus Subtilis 168”, Applied Microbiology and Biotechnology, 74, 3, 640-649, 2007. Dil Türkçe
Başak, A.N., “The Molecular Pathology of Beta Thalassemia in Turkey: the Boğaziçi University Experience”, Hemoglobin, 31, 2, 233-241, 2007. Dil Türkçe
Ozansoy, M., Başak, A.N., “Tauopathies: A Distinct Class of Neurodegenerative Diseases”, Balkan Journal of Medical Genetics, 10, 2, 3-14, 2007. Dil Türkçe
