A Newborn with Arhinia: Suspected BAM Syndrome by Coşkun Armağan, Tuğba Üçüncü Egeli, Can Akyıldız, Kadri Murat Erdoğan, Funda Erdoğan, Nuray Duman, Hasan Özkan

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A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies by Hacer Ergin, C Nur Semerci, Mevlüt Bican, Füsun Düzcan, A Baki Yagci, Kadri Murat Erdogan, A Cevik Tufan

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Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review by Özge Köprülü, Sezer Acar, Kadri Murat Erdoğan, Özlem Nalbantoğlu, Tarık Kırkgöz, Gülçin Arslan, Beyhan Özkaya, Yaşar Bekir Kutbay, Behzat Özkan

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First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss by Berk Özyılmaz, Gül Caner Mercan, Özgür Kırbıyık, Taha Reşid Özdemir, Samira Özkara, Özge Özer Kaya, Yaşar Bekir Kutbay, Kadri Murat Erdoğan, Merve Saka Güvenç, Altuğ Koç

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Prognostic and predictive role of liquid biopsy in lung cancer patients by Tuncay Goksel, Tuncay Goksel, Su Özgür, Aslı Tetik Vardarlı, Aslı Tetik Vardarlı, Altuğ Koç, Haydar Soydaner Karakuş, Haydar Soydaner Karakuş, Taha Reşid Özdemir, Kadri Murat Erdoğan, Ceyda Aldağ, Ceyda Aldağ, Ali Veral, Berna Komurcuoglu, Pınar Gursoy, Mehmet Emin Arayici, Asim Leblebici, Türkan Yiğitbaşı, Hülya Ellidokuz, Yasemin Basbinar

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