Genetics in Ophthalmology II–Anterior Segment Diseases by Canan Aslı Utine, Gülen Eda Utine

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Genetics in Ophthalmology I - Basic Concepts by Canan Aslı Utine, Gülen Eda Utine

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Congenital Cataract and Its Genetics: The Era of Next-Generation Sequencing by Hande Taylan Şekeroğlu, Gülen Eda Utine

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A case of Sotos syndrome with 5q35 microdeletion and novel clinical findings by Esra Kılıç, Gülen Eda Utine, Koray Boduroğlu

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A Baseline Algorithm for Molecular Diagnosis of Genetic Eye Diseases: Ophthalmologist’s Perspective by Hande Taylan Şekeroğlu, Gülen Eda Utine, Mehmet Alikaşifoğlu

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The Türkiye-Syria Earthquake: a response from the editors of the Turkish Journal of Pediatrics by Ali Düzova, Sinem Akgül, Gülen Eda Utine, Yılmaz Yıldız

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Cowden syndrome with bronchial asthma by Yasemin Ozsürekci, Süleyman Tolga Yavuz, Yasemin Alanay, Gülen Eda Utine, Omer Kalayci

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Anauxetic dysplasia: A rare clinical entity by Özlem Akgün-Doğan, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, Koray Boduroğlu

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A de novo 11q23 deletion in a patient presenting with severe ophthalmologic findings, psychomotor retardation and facial dysmorphism by Pelin Özlem Şimşek-Kiper, Yavuz Bayram, Gülen Eda Ütine, Yasemin Alanay, Koray Boduroğlu

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Gorlin Syndrome in Eleven Patients by Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, Koray Boduroğlu, Mehmet Alikaşifoğlu, Ergül Tunçbilek

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The rare reason of pain in hip girdle: Mucolipidosis type 3 gamma by Abdulkerim Kolkıran, Beren Karaosmanoğlu, Zihni Ekim Taşkıran, Pelin Özlem Şimşek-Kiper, Gülen Eda Utine

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Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes by Pelin Ozlem Simşek, Gülen Eda Utine, Ayfer Alikaşifoğlu, Yasemin Alanay, Koray Boduroğlu, Nurgün Kandemir

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Congenital partial arhinia: a rare malformation of the nose coexisting with holoprosencephaly by Sahin Takcı, Ayşe Korkmaz, Pelin Ozlem Simşek-Kiper, Gülen Eda Utine, Koray Boduroğlu, Murat Yurdakök

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Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene by Esra Kılıç, İlker Ertuğrul, Sema Özer, Mehmet Alikaşifoğlu, Dilek Aktaş, Koray Boduroğlu, Gülen Eda Ütine

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A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype by Pelin Ozlem Simşek-Kiper, Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, Mehmet Alikaşifoğlu, Koray Boduroğlu

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Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients by Gülen Eda Utine, Tolga Celik, Yasemin Alanay, Mehmet Alikaşifoğlu, Koray Boduroğlu, Ergül Tunçbilek, Dilek Aktaş

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Peters Plus syndrome: a recognizable clinical entity by Gizem Ürel Demir, Naz Güleray Lafcı, Özlem Akgün Doğan, Pelin Özlem Şimşek-Kiper, Gülen Eda Utine

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Polyposis deserves a perfect physical examination for final diagnosis: Bannayan-Riley-Ruvalcaba syndrome by Hayriye Hızarcıoğlu-Gülşen, Esra Kılıç, Elena Dominguez-Garrido, Yusuf Aydemir, Gülen Eda Utine, İnci Nur Saltık-Temizel

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Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome by Burçak Bilgin, Serkan Kabaçam, Ekim Taşkıran, Pelin Özlem Şimşek-Kiper, Yasemin Alanay, Koray Boduroğlu, Gülen Eda Utine

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A very rare case of a newborn with tetrasomy 9p and literature review by Merve Süleyman, Sümeyra Oğuz, Gözdem Kaykı, Hasan Tolga Çelik, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, Şule Yiğit

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