Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation von Sarıkaya, Emre, Kendirci, Mustafa, Demir, Mikail, Dündar, Munis

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Current and Future Therapeutic Strategies for Limb Girdle Muscular Dystrophy Type R1: Clinical and Experimental Approaches von Şahin, İzem Olcay, Özkul, Yusuf, Dündar, Munis

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Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift von Emeklİ, Rabia, İsmaİloğullari, Sevda, Bayram, Arslan, Akalin, Hilal, Tuncel, Gülten, Dündar, Munis

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Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy von Kahraman, Neslihan Sinim, Oner, Ayse, Ozkul, Yusuf, Dundar, Munis

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Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome von Dündar, Munis, Müller, Thomas, Zhang, Qi, Pan, Jing, Steinmann, Beat, Vodopiutz, Julia, Gruber, Robert, Sonoda, Tohru, Krabichler, Birgit, Utermann, Gerd, Baenziger, Jacques U., Zhang, Lijuan, Janecke, Andreas R.

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A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X): A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X) von Aydoğan, Kübra, Öztürk, Selcan, Dündar, Munis, Gümüş, Hakan, Saatçi, Çetin, Per, Hüseyin

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Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations von Öztürk, Selcan, Güleç, Ayten, Erdoğan, Murat, Demir, Mikail, Canpolat, Mehmet, Gümüş, Hakan, Çağlayan, Ahmet Okay, Dündar, Munis, Per, Hüseyin

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Ameliorative effects of pentoxifylline on NOS induced by diabetes in rat kidney von Sönmez, Mehmet Fatih, Dündar, Munis

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Current Advances in Breast Cancer: Implications for Developing New Treatment Strategies Through Epi-Drugs on the Road to Modifying the Epigenome von Kenanoğlu, Sercan

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A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort von ŞAHİN, İzem Olcay, KARATAŞ, Emine, DEMİR, Mikail, TAN, Büşra, PER, Hüseyin, ÖZKUL, Yusuf, DÜNDAR, Munis

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The frequencies of Y chromosome microdeletions in infertile males von Akınsal, Emre Can, Baydilli, Numan, Dündar, Munis, Ekmekçioğlu, Oğuz

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The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, an... von Alzaidi, Zahraa, Yildiz, Şule Menziletoğlu, Saatçi, Çetin, Akalin, Hilal Ünlü, Muderris, Iptisam Ipek, Aynekin, Buşra, Şahin, Izem Olcay, Dündar, Munis

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A Potential Method to Help Predict Genetic Diseases and Arrange Healthcare: Copy Number Variation Analysis von Munis Dündar, Arslan, Saide Betül

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Loss of dermatan-4-sulfotransferase 1 (D4ST1/CHST14) function represents the first dermatan sulfate biosynthesis defect, "dermatan sulfate-deficient adducted thumb-clubfoot syndrom... von Janecke, Andreas R., Baenziger, Jacques U., Müller, Thomas, Dündar, Munis

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Mesenchymal stem cells from adipose tissue prone to lose their stemness associated markers in obesity related stress conditions von Al-Sammarraie, Sura Hilal Ahmed, Ayaz-Güner, Şerife, Acar, Mustafa Burak, Şimşek, Ahmet, Sınıksaran, Betül Seyhan, Bozalan, Habibe Damla, Özkan, Miray, Saraymen, Recep, Dündar, Munis, Özcan, Servet

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The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity von Yüksekkaya, Mehmet, Tutar, Nuri, Büyükoğlan, Hakan, Dündar, Munis, Yılmaz, İnsu, Gülmez, İnci, Oymak, Fatma Sema, Balta, Burhan, Korkmaz, Keziban, Demir, Ramazan

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Research of genetic bases of hereditary non-syndromic hearing loss von Subaşıoğlu, Aslı, Duman, Duygu, Sırmacı, Aslı, Bademci, Güney, Carkıt, Fehime, Somdaş, Mehmet Akif, Erkan, Mustafa, Tekin, Mustafa, Dündar, Munis

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A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions von Günay, Neslihan, Pınarbaşı, Ayşe Seda, Doğan, Muhammet Ensar, Yel, Sibel, Balaban, Aynur Gencer, Dursun, İsmail, Eken, Ahmet, Akgün, Hülya, Dündar, Munis, Poyrazoğlu, Muammer Hakan

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A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers von Günay, Neslihan, Pınarbaşı, Ayşe Seda, Doğan, Muhammet Ensar, Yel, Sibel, Balaban, Aynur Gencer, Dursun, İsmail, Eken, Ahmet, Akgün, Hülya, Dündar, Munis, Poyrazoğlu, Muammer Hakan

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Evaluation of aortic intima-media thickness in newborns with Down syndrome von Sarici, Dilek, Kurtoglu, Selim, Sarici, Serdar Umit, Yikilmaz, Ali, Akin, Mustafa Ali, Gunes, Tamer, Ozturk, Mehmet Adnan, Narin, Nazmi, Dündar, Munis, Serdar, Muhittin

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