Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population von Kilic, S., Ozdemir, O., Silan, F., Isik, S., Yildiz, O., Karaagacli, D., Silan, C., Ogretmen, Z.

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

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Effects of Cyp2c19 and P2y12 Gene Polymorphisms on Clinical Results of Patients Using Clopidogrel After Acute Ischemic Cerebrovascular Disease von Sen, H. M., Silan, F., Degirmenci, Y., Kamaran, Ozisik H. I.

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Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia von Djurovic, J., Stojkovic, O., Ozdemir, O., Silan, F., Akurut, C., Todorovic, J., Savic, K., Stamenkovic, G.

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The MEFV gene pathogenic variants and phenotype-genotype correlation in children with familial Mediterranean fever in the Çanakkale population von Battal, F, Silan, F, Topaloğlu, N, Aylanç, H, Yıldırım, Ş, Köksal Binnetoğlu, F, Tekin, M, Kaymaz, N, Ozdemir, O

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Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey von Uludağ, A, Uysal, A, Uludağ, A, Ertekin, YH, Tekin, M, Kütük, B, Silan, F, Özdemir, Ö

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SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism von Borozdin, W, Boehm, D, Leipoldt, M, Wilhelm, C, Reardon, W, Clayton-Smith, J, Becker, K, Mühlendyck, H, Winter, R, Giray, Ö, Silan, F, Kohlhase, J

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Double translocation: an interesting family history von Uysal, A, Uludağ, A, Sılan, F, Erçelen, N, Zafer, C, Ozdemir, O

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Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations von Ozdemir, Oztürk, Yenicesu, Gonca Imir, Silan, Fatma, Köksal, Binnur, Atik, Sinem, Ozen, Filiz, Göl, Mert, Cetin, Ali

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Vitamin D Receptor Gene BSMI, FOKI, APAI, and TAQI Polymorphisms and the Risk of Atopic Dermatitis von Kilic, S, Silan, F, Hiz, M M, Isik, S, Ogretmen, Z, Ozdemir, O

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A new mutation of the fukutin gene in a non-Japanese patient von Silan, Fatma, Yoshioka, Mieko, Kobayashi, Kazuhiro, Simsek, Enver, Tunc, Murat, Alper, Murat, Cam, Meryem, Guven, Aysel, Fukuda, Yoji, Kinoshita, Moritoshi, Kocabay, Kenan, Toda, Tatsushi

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Association between FokI , ApaI and TaqI RFLP polymorphisms in VDR gene and H ashimoto's thyroiditis: preliminary data from female patients in S erbia von Djurovic, J., Stojkovic, O., Ozdemir, O., Silan, F., Akurut, C., Todorovic, J., Savic, K., Stamenkovic, G.

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PP-288 Intercellular Adhesion Molecule-1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow von Gazi, E, Barutçu, A, Altun, B, Temiz, A, Bekler, A, Urfalı, M, Sılan, F, Çölkesen, Y, Özdemir, Ö

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Non‐Hodgkin's lymphoma and auricular hypoplasia: associated with juvenile colloid milium or ligneous conjunctivitis? von Kavak, A, Kaya, M, Alper, M, Çam, M, Büyükbabani, N, Bilen, A, Sılan, F

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Increased T-allele frequency of 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene in differentiated thyroid carcinoma von Ozdemir, Semra, Silan, Fatma, Hasbek, Zekiye, Uludag, Ahmet, Atik, Sinem, Erselcan, Taner, Ozdemir, Ozturk

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Combined effect of Factor V Leiden, MTHFR, and angiotensin-converting enzyme (insertion/deletion) gene mutations in hypertensive adult individuals: a population-based study from Si... von Demirel, Yeltekin, Dogan, Sezai, Uludag, Ahmet, Silan, Coskun, Atik, Sinem, Silan, Fatma, Ozdemir, Ozturk

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Prevalence and mutations of [beta]-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey von Uludag, A, Uysal, A, Ertekin, YH, Tekin, M, Kütük, B, Silan, F, Özdemir, Ö

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The Proto-Oncogene KRAS and BRAF Profiles and Some Clinical Characteristics in Colo rectal Cancer in the Turkish Population von Ozen, F, Ozdemir, S, Zemheri, E, Hacimuto, G, Silan, F, Ozdemir, O

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Congenital sialoblastoma (embryoma) associated with premature centromere division and high level of alpha-fetoprotein von Ozdemir, Ismail, Simsek, Enver, Silan, Fatma, Demirci, Fuat

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Does the maxillary sinus have a triggering role in nasal nitric oxide synthesis? von GÜCLÜ, Oguz, ULUDAG, Ahmet, AKCALI, Alper, TEKIN, Kazim, ERDOGAN, Halil, SILAN, Fatma, SEFA DEREKÖY, Fevzi

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