Effects of CYP2C19 and P2Y12 Gene Polymorphisms on Clinical Results of Patients Using Clopidogrel after Acute Ischemic Cerebrovascular Disease

Por Sen, HM, Silan, F, Silan, C, Degirmenci, Y, Ozisik Kamaran, HI
Publicado no Balkan J Med Genet (2015)

Double Translocation: An Interesting Family History

Por Uysal, A, Uludağ, A, Sılan, F, Erçelen, N, Zafer, C, Özdemir, Ö
Publicado em 201

Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey

Por Uludağ, A, Uysal, A, Uludağ, A, Ertekin, YH, Tekin, M, Kütük, B, Silan, F, Özdemir, Ö
Publicado no Balkan J Med Genet (2016)

The MEFV Gene Pathogenic Variants and Phenotype-genotype Correlation in Children with Familial Mediterranean Fever in the Çanakkale Population

Por Battal, F, Silan, F, Topaloğlu, N, Aylanç, H, Yıldırım, Ş, Köksal Binnetoğlu, F, Tekin, M, Kaymaz, N, Ozdemir, O
Publicado no Balkan J Med Genet (2016)

SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism

Por Borozdin, W, Boehm, D, Leipoldt, M, Wilhelm, C, Reardon, W, Clayton-Smith, J, Becker, K, Muhlendyck, H, Winter, R, Giray, O, Silan, F, Kohlhase, J
Publicado em 2004

A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN

Por Lehmann, K. , Seemann, P. , Silan, F. , Goecke, T. O. , Irgang, S. , Kjaer, K. W. , Kjaergaard, S. , Mahoney, M. J. , Morlot, S. , Reissner, C. , Kerr, B. , Wilkie, A. O. M. , Mundlos, S. 
Publicado em 2007