A case of familial recurrent 17q12 microdeletion syndrome presenting with severe diabetic ketoacidosis by Can Aydın, Eylem Kıral, Ezgi Susam, Aslı Kavaz Tufan, Coskun Yarar, Nuran Çetin, Sinem Kocagil, Birgül Kırel

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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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