Do CCR5 (CCR5Δ32) and TLR3 (RS5743313) gene polymorphisms prevent chronic hepatitis B infection? von Tuncel, Burçin, Kaygusuz, Sedat, Sayın Kocakap, Derya Beyza, Aksoy, Emel, Azkur, Ahmet Kürşat

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Clinical significance of MEFV gene variation R202Q von Kandur, Yaşar, Kocakap, Derya Beyza Sayın, Alpcan, Aysegul, Tursun, Serkan

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Adverse effect of VEGFR-2 (rs1870377) polymorphism on the clinical course of COVID-19 in females and males in an age-dependent manner von Sayın Kocakap, Derya Beyza, Kaygusuz, Sedat, Aksoy, Emel, Şahin, Ömer, Baççıoğlu, Ayşe, Ekici, Aydanur, Kalpaklıoğlu, Ayşe Füsun, Ekici, Mehmet Savaş, Gül, Serdar, Kaçmaz, Birgül, Ayaşlıoğlu Açıkgöz, Ergin, Alyılmaz Bekmez, Sibel, Rouse, Barry T, Azkur, Ahmet Kürşat

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The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of Turkey von Sayın Kocakap, Derya Beyza, Günel-Özcan, Ayşen, Çabuk, Feryal, Ensari, Cüneyt

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The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its dependence on gender von Sayın Kocakap, Derya Beyza, Doğru, Mehmet Tolga, Şimşek, Vedat, Çabuk, Feryal, Yıldırım, Nesligül, Çelik, Yunus, Alyılmaz Bekmez, Sibel, Erdem, Solmaz

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A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis von Şenbil, Nesrin, Arslan, Zeynep, Sayın Kocakap, Derya Beyza, Bilgili, Yasemin

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Interleukin (IL)-17F (H161R) and IL-23R (R381Q) Gene Polymorphisms in Turkish Population with Periodontitis von Erdemir, Ebru, Hendek, Meltem, Kocakap, Derya, Ozkan, Serdar

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A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis von Şenbil, Nesrin, Arslan, Zeynep, Sayın Kocakap, Derya Beyza, Bilgili, Yasemin

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