A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant von Deliloğlu, Burak, Özkan, Hasan, Duman, Nuray, Yılmaz, Şebnem, Durmaz, Asude, Ceylan, Emine İpek, Aykut, Ayça, Tüzün, Funda, Tüfekçi, Özlem, Ören, Hale

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Comprehensive analysis of genotypic and phenotypic characteristics of biotinidase deficiency patients in the eastern region of Türkiye von Çıkı, Kısmet, Alavanda, Ceren, Ceylan, Emine İpek, Tanyalçın, Tijen, Kılavuz, Sebile

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Vitamin D receptor gene polymorphisms in ocular surface squamous cell neoplasms von Ismayilova, Nergiz, Palamar, Melis, Onay, Huseyin, Ceylan, Emine Ipek, Atik, Tahir, Akalin, Taner, Yagci, Ayse

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A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation von Kılavuz, Sebile, Basaranoglu, Murat, Epcacan, Serdar, Bako, Derya, Ozer, Arife, Donmez, Yasemin Nuran, Ceylan, Emine Ipek, Tukun, Ajlan, Ceylaner, Serdar, Geylani, Hadi, Mungan, Halise Neslihan Onenli

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FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis von Ceylan, Emine Ipek, Solmaz, Asli Ece, Onay, Huseyin, Aykut, Ayca, Durmaz, Asude, Yesil, Gozde, Hazan, Filiz, Kiraz, Aslihan, Tuysuz, Beyhan, Gunes, Meltem Cerrah

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FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis von Ceylan, Emine İpek, Aslı Ece Solmaz, Onay, Hüseyin, Aykut, Ayça, Durmaz, Asude, Yeşil, Gözde, Hazan, Filiz, Kiraz, Aslıhan, Tüysüz, Beyhan, Meltem Cerrah Güneş

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Investigation of hematologic findings related to brucellosis in Anatolian region von Selik, Mehmet, Arslan, Yusuf, Topcu, Ertugrul, Sahinoglu, Mustafa Serhat, Altindag, Deniz, Gurbuz, Esra

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