Early-onset Chronic Keratitis as the First Presenting Component of Autoimmune Polyendocrine Syndrome Type 1: A Case Report and Review of the Literature by Enver Şimşek, Tülay Şimşek, Oğuz Çilingir

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Prevalence of Nonclassic Congenital Adrenal Hyperplasia in Turkish Children Presenting with Premature Pubarche, Hirsutism, or Oligomenorrhoea by Cigdem Binay, Enver Simsek, Oguz Cilingir, Zafer Yuksel, Ozden Kutlay, Sevilhan Artan

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Apolipoprotein E allelic variants and cerebral palsy by Evren Gümüş, Beyhan Durak Aras, Oğuz Çilingir, Coşkun Yarar, Kürşat Bora Çarman, Sibel Laçiner-Gürlevik, Ozan Koçak, Sevilhan Artan

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Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies by M. Arda Temena, Ebru Erzurumluoglu Gokalp, Ezgi Susam, Duygu Cinar, Hikmet Kiztanir, Pelin Kosger, Beyhan Durak Aras, Sevilhan Artan, Oguz Cilingir

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Evaluation of Genomic Variants in Non-syndromic Congenital Heart Disease in Turkish Pediatric Group by Sinem Kocagil, Büşra Özkan, Sabri Aynacı, Tuğçem Akın, Ezgi Susam, Ebru Erzurumluoğlu Gökalp, Beyhan Durak Aras, Birsen Uçar, Sevilhan Artan, Oğuz Çilingir

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Chromosomal abnormalities in couples with recurrent pregnancy loss: a 16-year cross-sectional study of 4030 cases from Turkey by Sabri Aynaci, Sinem Kocagil, Efsun Tosumoglu, Ezgi Susam, Betul Kilic, Ebru Erzurumluoglu Gokalp, Oguz Cilingir, Beyhan Durak Aras, Basar Tekin, Sevilhan Artan

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Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients by Taner Ulus, Muhammet Dural, Pelin Meşe, Furkan Yetmiş, Kadir Uğur Mert, Bülent Görenek, Oğuz Çilingir, Ebru Erzurumluoglu Gökalp, Serap Arslan, Sevilhan Artan, Özlem Aykaç, Ertuğrul Çolak, Hikmet Yorgun, Uğur Canpolat, Kudret Aytemir

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