C., S., Sılan., F., Doğan., Ö., Özdemir, S., Uludağ, A., Atik, S., Güngör, B., Akdur, S., Aksulu, H.E., Özdemir, Ö. () "Türk popülasyonunda antikoagülan tedavi kullanımı gereken hastalarda VKORC1 1639 G A ve CYP2C9 2 ve 3 genotipleri", 21. Ulusal Farmakoloji Kongresi, Eskişehir , Türkiye
V., T., Sılan., C., Akdur., S., Özdemir, S., Uludağ, A., Atik, S., Sılan, F., Özdemir, Ö. () "Mitokondrial A1555G mutasyonunun sağırlık etiyolojisindeki yeri ve aminoglikozid toksisitesi ile ilişkisi", 21. Ulusal Farmakoloji Kongresi , Türkiye
B., K., M., S., K., K., M, T., H, Ö., Ş, Ç., İ, S., Ö, Ö. () "Kolorektal kanserde tümör süpresör HIC1 SFRP2 p16 DAPK1 ve MGMT genlerinin promoter hipermetilasyon frekansları Türkiye Klinikleri Journal of Medical Sciences", Kolorektal kanserde tümör süpresör HIC1, SFRP2, p16, DAPK1 ve MGMT genlerinin promoter hipermetilasyon frekansları. Türkiye Klinikleri Journal of Medical Sciences , Türkiye
S., S., EF., P., İ, Ö.Ö.A.S. () "A 46 XXdel X p22 1 22 2 case relevant to its clinical findings", Abstracts of the 1th Eurepean Cytogenetics Conference
Ö., Ö., EF., P., İ., S., A, S.S.A.Ç. () "Short stature and other clinical findings of a case with karyotype 46 XYdel Y q11 2 12 mar", Abstracts of the 1th Eurepean Cytogenetics Conference.
Ö., Ö., EF., P., İ, S. () "Chromosome 2 fragility in 48 XXYY syndrome", Second European Cytogenetics Conference
İ., S., Ö., Ö., S., S., F, P. () "Two siblings Androgen Insensitivity Syndrome with 45 XY t 13q 14q and one is normal 46 XY karyotipes Three case reports", Annual Metting of the European Society of Human Genetics
A., Ç., T., E., S., S., S, Ö., D, O., Ö, Ö. () "Increased sister chromatide exchange frequency in tyroid cancer patients that treated with I1313 previous results of one case", Third European Conference
I., S., F., P., T., G., A, C., E, C., E, G., O, K.N.A.O. () "Molecular and cytogenetic characterisation of a female of hypoplastic external genitalia with a familial Y 21 translocation", 5.th Euoropean Cytogenetics Conference, Madrid, SPAIN.
O., O., A., O., C., D., E, G., S, Y., A, C., G, B., B, K., D, O. () "The SSCP profiles of mutated homeobox PAX9 gene in orofacial clefts in human", 5.th Euoropean Cytogenetics Conference,Madrid, SPAIN.
I., S., A., C., E., C., F, O., N, K., M, E., O, O. () "Chromosome 7 duplication in a young girl with congenital heart disease unusual behaviours and low IQ level clinical and cytogenetical characterisation", European Human Genetics conference Amsterdam, The Netherlands
O., O., E., Y., S., A., E, G., G, G., OF, G., EY, G. () "Mutated SSCP profiles of c myc proto oncogene in bladder s papillary urothelial transitional cell neoplasms", A molecular approach to cell prolifeCHROMOSOME RESEARCH
EE., A., I., S., A., B., B, K.H.K., O, M.S.A.O. () "Heterozygous deletion of exon 8 in WFS1 gene in two Wolfram Syndrome probands with hearing loss", 7th European Cytogenetics Conference
M., S., O., O., A., C., M, T., S, A., D, O., B, Y.Y.A.K. () "The combined effect of K ras proto oncogene and promoter hypermethylation of tumor supressor SFRP2 gene in a case with mucinous anal carcinoma A case report", 7th European Cytogenetics Conference
O., O., E., Y., S., A., E, G., G, G., F, Y., B, K., F, G., EY, G. () "Epigenetik alterations and oncogenes mutations in urinary bladder carcinoma", 7th European Cytogenetics Conference
HK., K., S., M., A., U., N, K., O, K., F, Y., O, B.O.A.O. () "The crucial role of MDR1 ABCB1 gene polymorphism in abdominal aortic aneurysm A preliminary results of a pilot study", 7th European Cytogenetics Conference
S., A., T., D., B., K., ME, Y., C, G., S, E., O, A.I.A.O. () "Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report", 7th European Cytogenetics Conference
., K.N., ., O.F., ., K.R., I, S., O, O. () "CRUCIAL ROLE OF PARENTAL MTHFR GENE POLYMORPHISM INVOLVED IN HOMOCYSTEINE METABOLISM IN DOWN SYNDROME", IUBMB LIFE
Kocak., , Ozen., N., Arslan., F., MS, , O, O. () "ETERMINATION OF DISTRIBUTION OF COMMON MEFV GENE MUTATIONS IN HEALTHY INDIVIDUALS WHO HAD BEEN EXPOSED TO APPENDECTOMY IN CHILDHOOD AGE", IUBMB LIFE
