A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN by 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 by 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 by 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 by 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 by 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 by 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 by Uysal, A, Uludağ, A, Sılan, F, Erçelen, N, Zafer, C, Ozdemir, O

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A new mutation of the fukutin gene in a non-Japanese patient by 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 by 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 by 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? by Kavak, A, Kaya, M, Alper, M, Çam, M, Büyükbabani, N, Bilen, A, Sılan, F

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

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

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Topic: Rare and Special Cases, The Real “Strange Cases” by Zarrinkhoo, E., Miller, J., Walker, A., Weisman, M., Towfigh, S., Tushev, R., Petkov, I., Tsutsumi, G., Morua, A. Garcia, Bravo, R., Azcarate, A., Zavala, H., Radu, E. V., David, O. I., Stoian, A. R., Strambu, V. E., Iancu, C., Gheorghiu, L. I., Grigorean, V. T., Lupascu, C., Straja, D. N., Iacobini, M. A., Ponten, J., Nienhuijs, S., Permekerlis, A., Petousis, S., Miroforidis, A., Milias, K., Kouridakis, P., Park, J., Kim, D., Suzuki, H., Watanabe, M., Uchida, E., Nakanaga, H., Irie, S., Minamimura, K., Kobayashi, T., Hirata, T., Mafune, K., Milosevic, P., Light, D., Aawsaj, Y., Horgan, L., Latham, L., Ceriani, I., Livraghi, L., Berselli, M., Gambitta, B., Galvanin, J., Cotronea, C., Farassino, L., Crespi, A., Cocozza, E., Kulic, V., Matkovic, M., Percevic, G., Katayama, T., Kumata, Y., Ogawa, E., Horikawa, M., Fukushima, R., Jaroszewski, D., Johnson, K., Harold, K., Kumata, M., Guarnieri, F., Smaldone, W., Gaspard, M., Bomben, F., Gamarra, M. Florez, Olivero, C. Fraile, Martinez, M. Josa, Contin, M. Perez, Jiménez-Valladolid, D., Torres García, A., Descloux, A., Schramm, B., Schneider, U., Nocito, A., Navarrete, M. Cesardo, Ortega, N., Bergamini, S., Semeraro, C., Cano, M. Lopez, Torrecilla, N. Ortega, Cavallaro, G., Iorio, O., Avallone, M., Ruscio, S., Silecchia, G., Butron, T., Sopeña, R., Silan, F., Garcia, V., Bernal, J., Ortiz, M., Guadarrama, J., Shirai, K., Lomas, M.

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Protective effect of melatonin on β-cell damage in streptozotocin-induced diabetes in rats by Yavuz, Ozlem, Cam, Meryem, Bukan, Neslihan, Guven, Aysel, Silan, Fatma

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A novel L1CAM mutation with L1 spectrum disorders by Silan, Fatma, Ozdemir, Ismail, Lissens, Willy

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Incontinentia pigmenti with NEMO mutation in a Turkish family by Silan, Fatma, Aydogan, Ilker, Kavak, Ayse, Bardaro, Tiziano, D’Urso, Michele

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Syndromic etiology in children at schools for the deaf in Turkey by Silan, Fatma, Demirci, Levent, Egeli, Ayten, Egeli, Erol, Onder, Halil Ibrahim, Ozturk, Ozcan, Unal, Zehra Seda

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Evaluation of deaf children in a large series in Turkey by Ozturk, Ozcan, Silan, Fatma, Oghan, Fatih, Egeli, Erol, Belli, Seyda, Tokmak, Abdurrahman, Egeli, Ayten, Harputluoglu, Ugur, Onder, Halil Ibrahim, Zafer, Cansu

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Etiology of deafness at the Yeditepe School for the deaf in Istanbul by Egeli, Erol, Çiçekci, Günferi, Silan, Fatma, Öztürk, Özcan, Harputluoğlu, Uğur, Onur, Aşkin, Egeli, Ayten, Yildiz, Aysel

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