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	1.	A Rare Double Aneuploidy Case (Down-Klinefelter). [electronic resource] by Bozdogan, Sevcan Tug Bisgin, Atil Publication details: Journal of pediatric genetics Dec 2017 In: Journal of pediatric genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features. [electronic resource] by Incecik, Faruk Besen, Seyda Bozdogan, Sevcan Tug Publication details: Annals of Indian Academy of Neurology In: Annals of Indian Academy of Neurology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel mutation of ROBO3 in horizontal gaze palsy with progressive scoliosis. [electronic resource] by Bozdoğan, Sevcan Tuğ Dinç, Erdem Sarı, A Ayça Özgür, Anıl Bişgin, Atıl Producer: 20171117 In: Ophthalmic genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children. [electronic resource] by Bozdogan, Sevcan Tug Kutuk, Meryem Ozlem Tufan, Evren Altıntaş, Zuhal Temel, Gülhan Orekici Toros, Fevziye Publication details: Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology Nov 2018 In: Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Alpha-thalassemia mutations in adana province, southern Turkey: genotype-phenotype correlation. [electronic resource] by Bozdogan, Sevcan Tug Yuregir, Ozge Ozalp Buyukkurt, Nurhilal Aslan, Huseyin Ozdemir, Zeynep Canan Gambin, Tomasz Producer: 20150331 In: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	The Prevalence of Gap Junction Protein Beta 2 (GJB2) Mutations in Non Syndromic Sensorineural Hearing Loss in Çukurova Region. [electronic resource] by Bozdoğan, Sevcan Tuğ Kuran, Gökhan Yüregir, Özge Özalp Aslan, Hüseyin Haytoğlu, Süheyl Ayaz, Akif Arıkan, Osman Kürşat Producer: 20151030 In: The journal of international advanced otology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish cases. [electronic resource] by Bozdogan, Sevcan Tug Unsal, Cagatay Erkman, Hakan Genc, Ahmet Yuregir, Ozge Ozalp Muslumanoglu, Muhammed Hamza Aslan, Huseyin Producer: 20121009 In: Hemoglobin vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	β-Globin chain abnormalities with coexisting α-thalassemia mutations. [electronic resource] by Guvenc, Birol Canataroglu, Abdullah Unsal, Cagatay Yildiz, Sule Menziletoglu Turhan, Ferda Tekin Bozdogan, Sevcan Tug Dincer, Suleyman Erkman, Hakan Producer: 20121012 In: Archives of medical science : AMS vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	β-Thalassemia mutations and hemoglobinopathies in Adana, Turkey: results from a single center study. [electronic resource] by Guvenc, Birol Canataroglu, Abdullah Unsal, Cagatay Yildiz, Sule Menziletoglu Turhan, Ferda Tekin Bozdogan, Sevcan Tug Dincer, Suleyman Erkman, Hakan Producer: 20121002 In: Archives of medical science : AMS vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin. [electronic resource] by Bayram, Yavuz Karaca, Ender Coban Akdemir, Zeynep Yilmaz, Elif Ozdamar Tayfun, Gulsen Akay Aydin, Hatip Torun, Deniz Bozdogan, Sevcan Tug Gezdirici, Alper Isikay, Sedat Atik, Mehmed M Gambin, Tomasz Harel, Tamar El-Hattab, Ayman W Charng, Wu-Lin Pehlivan, Davut Jhangiani, Shalini N Muzny, Donna M Karaman, Ali Celik, Tamer Yuregir, Ozge Ozalp Yildirim, Timur Bayhan, Ilhan A Boerwinkle, Eric Gibbs, Richard A Elcioglu, Nursel Tuysuz, Beyhan Lupski, James R Producer: 20160708 In: The Journal of clinical investigation vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes. [electronic resource] by Yuan, Bo Pehlivan, Davut Karaca, Ender Patel, Nisha Charng, Wu-Lin Gambin, Tomasz Gonzaga-Jauregui, Claudia Sutton, V Reid Yesil, Gozde Bozdogan, Sevcan Tug Tos, Tulay Koparir, Asuman Koparir, Erkan Beck, Christine R Gu, Shen Aslan, Huseyin Yuregir, Ozge Ozalp Al Rubeaan, Khalid Alnaqeb, Dhekra Alshammari, Muneera J Bayram, Yavuz Atik, Mehmed M Aydin, Hatip Geckinli, B Bilge Seven, Mehmet Ulucan, Hakan Fenercioglu, Elif Ozen, Mustafa Jhangiani, Shalini Muzny, Donna M Boerwinkle, Eric Tuysuz, Beyhan Alkuraya, Fowzan S Gibbs, Richard A Lupski, James R Producer: 20150410 In: The Journal of clinical investigation vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)