A 10.46Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism von Soysal, Yasemin, Vermeesch, Joris, Davani, Nooshin Ardeshir, Hekimler, Kuyas, Imirzalioglu, Necat

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Human Papilloma Viruses and Their Genotype Distribution in Women with High Socioeconomic Status in Central Anatolia, Turkey: A Pilot Study von Barut, Mert Ulaş, Yildirim, Engin, Kahraman, Mehmet, Bozkurt, Murat, Imirzalioğlu, Necat, Kubar, Ayhan, Çalişkan, Eray, Sak, Sibel, Aksu, Tarık

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Age-related macular degeneration and association of CFH Y402H and LOC387715 A69S polymorphisms in a Turkish population von Soysal, Yasemin, Inan, Umit Übeyt, Küsbeci, Tuncay, Imirzalioğlu, Necat

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KLOTHO and VDR Gene Polymorphisms and Clinical Phenotype in Chronic Kidney Disease Patients von Öztürk,Kuyaş Hekimler, Yıldız,Saliha Handan, İmirzalıoğlu,Necat, Demir,Serap, Köken,Tülay, Ulu,Memnune Sena

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A 10.46 Mb 12p11.1–12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism von Soysal, Yasemin, Vermeesch, Joris, Davani, Nooshin Ardeshir, Hekimler, Kuyaş, İmirzalıoğlu, Necat

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Modulator effects of the methylenetetrahydrofolate reductase C677T polymorphism on response to vitamin B12 therapy and homocysteine metabolism von Sensoy, Nazli, Şoysal, Yasemin, Kahraman, Ahmet, Doğan, Nurhan, Imirzalioğlu, Necat

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Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy von Soysal, Yasemin, Balcı, Sevim, Hekimler, Kuyaş, Liehr, Thomas, Ewers, Elisabeth, Schoumans, Jacqueline, Bui, The‐Hung, İçduygu, Fadime Mutlu, Kosyakova, Nadezda, İmirzalıoğlu, Necat

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A Case with Mosaic Ring Chromosome 18 von Samli, Hale

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Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues von Barut, Mert Ulaş, Bozkurt, Murat, Kahraman, Mehmet, Yıldırım, Engin, Imirzalioğlu, Necat, Kubar, Ayhan, Sak, Sibel, Ağaçayak, Elif, Aksu, Tarık, Çoksüer, Hakan

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New heritable fragile site at 15q13 in both members of a nonconsanguineous couple von Karadeniz, Nadide Nilüfer, Tunca, Yusuf, Imirzalıoğlu, Necat

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Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture von Samli, Hale, Solak, Mustafa, Imirzalioǧlu, Necat, Beyatlı, Yavuz, Şimşek, Solmaz, Kahraman, Semra

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Investigating the in vitro effect of taurine on the infant lymphocytes by sister chromatid exchange von ERGUN, MEHMET ALI, SOYSAL, YASEMIN, KISMET, EROL, AKAY, CEMAL, DUNDAROZ, RUSEN, ILHAN, MUSTAFAN, IMIRZALIOGLU, NECAT

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Complete atrioventricular block in becker muscular dystrophy: A case report von UYAN, Cihangir, YAZICI, Mehmet, AKDEMİR, Ramazan, İMİRZALİOĞLU, Necat

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Cinsel farklılaşma bozukluğu olan olgularda genetik yaklaşım von TAŞÇILAR, M. Emre, SAMEDLİ, Samed, TORUN, Deniz, KOZAN, Salih, BAHÇE, Muhterem, GÜRAN, Şefik, İMİRZALIOĞLU, Necat, BOLU, Erol, GÜL, Davut, TUNCA, Yusuf

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The effects of folic acid application on IL-1β levels of human gingival fibroblasts stimulated by phenytoin and TNFα in vitro : a preliminary study von Dogan, Altan, Tunca, Yusuf, Özdemir, Atilla, Sengül, Ali, Imirzalioglu, Necat

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A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism von Soysal, Yasemin, Vermeesch, Joris, Ardeshir Davani, Nooshin, Hekimler, Kuyaş, Imirzalıoğlu, Necat

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The effects of folic acid application on IL-1beta levels of human gingival fibroblasts stimulated by phenytoin and TNFalpha in vitro: a preliminary study von Doğan, A, Tunca, Y, Ozdemir, A, Sengül, A, Imirzalioğlu, N

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An investigation of the effects of FGFR2 and B7-H4 polymorphisms in breast cancer von Özgöz, Asuman, Şamlı, Hale, Öztürk, Kuyaș, Orhan, Bülent, Içduygu, Fadime, Aktepe, Fatma, Imirzalioglu, Necat

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Analysis of PTEN gene mutations in a Turkish patient with Cowden syndrome von Soysal, Yasemin, Tate, Genshu, Polat, Coşkun, Polat, Nevriye, Aktepe, Fatma, Sivaci, Yaşar, Imirzalioglu, Necat

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Original Article: Investigating the in vitro effect of taurine on the infant lymphocytes by sister chromatid exchange von MEHMET ALI ERGUN, YASEMIN SOYSAL, EROL KISMET, CEMAL AKAY, RUSEN DUNDAROZ, MUSTAFAN ILHAN, Imirzalioglu, Necat

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