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	1.	A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathy. [electronic resource] by Tekin, Mustafa Akcayoz, Duygu Incesulu, Armagan Producer: 20050928 In: American journal of medical genetics. Part A vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population. [electronic resource] by Tekin, Mustafa Akcayoz, Duygu Ucar, Canan Gulen, Huseyin Akar, Nejat Producer: 20060221 In: Human biology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome. [electronic resource] by Ergür, Ayça T Ocal, Gönül Berberoglu, Merih Tekin, Mustafa Kiliç, Birim G Aycan, Zehra Kutlu, Alev Adiyaman, Pelin Siklar, Zeynep Akar, Nejat Sahin, Aynur Akçayöz, Duygu Producer: 20080710 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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