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
S., O., F., S., T., E., A, U., F, U., A, C., S, A., O, O. () "Increased T allele frequency in MTHFR C677T gene in thyroid carcinme", 8th European Cytogenetic Conference
O., O., H., A., M., T., S, O., M, K., B, K., F, O. () "The endemic RTL80V I and RTM204V I YMDD mutation profiles in a case of chronic hepatitis B", 8th European Cytogenetic Conference
D., K., O., O., E., K., S, O., B, K., EY, G. () "Epigenetic silencing of the tumor supressor HIC1 and SFRP2 genes in prostate carcinomas", European Cytogenetic Conference
S., A., F., O., C., S., A, U., F, C., F, S., S, O., O, O. () "Increased T allele frequency in multidrug transporter ABCB1 MDR1 gene in FMF patients of colchicine unresponsiveness", European Human Genetics Conference
O., O., Gİ., Y., F., S., M, Ç., B, K., S, A., F, Ö., M, G., A, Ç. () "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", European Human Genetics Conference
A., U., Y., D., AS., G., C, S., S, A., F, S., Ö, Ö. () "Combine effect of Factor V Leiden MTHFR and Angiotensin converting enzyme insertion deletion gene mutations in hypertensive adult individuals a population based study from Sivas and Canakkale TURKEY", European Human Genetics Conference
F., S., O., G., LE., K., C, S., S, A., A, U., A, D., FS, D., Ö, Ö. () "GJB2 35delG and Mitochondrial A1555G mutations and etiology of deafness at the Gelibolu School for the Deaf in Turkey", European Human Genetics Conference
E., E., O, O. () "Genome based transcriptome profile of some etiological parameters in breast cancer", Abstracts of the 2011 MASCC\ISOO Symposium
Silan., C., Dogan., O., Silan., F., Kukulguven, F., Asgun, H., Ozdemir, S., Uludag, A., SAtik, , Gungor, B., Akdur, S., Aksulu, H., Ozdemir, O. () "The prevalence of VKORC1 1639 G A and CYP2C9 2 3 genotypes in patients that requiring anticoagulant therapy in Turkish population", European Human GeneticsConference
Ozdemir., O., Alagozlu., H., Timucin, M. () "Strong association between ABCB1 gene MDR1 3435 C T polymorphism and multiple drug nonresponder patients of chronic hepatitis C", European Human Genetics Conference
Ozdemir., S., Uludag., A., Silan., F., Atik, S., Turgut, B., Ozdemir, O. () "The possible role of the xenobiotic transporter P glycoproteinpolymorphism that encoded by the MDR1 3435 C T gene in the susceptibility of differentiated thyroid cancer", European Human Genetics Conference
Uludag., A., Ozdemir., S., Silan., C., Uludag, A., Atik, S., Silan, F., Ozdemir, O. () "Evaluation of CYP2C9 CYP2C19 and CYP2D6 gene polymorphisms in thyroid cancer", European Human Genetics Conference
