Your search returned 6 results.

Results
	1.	Marked improvement in Segawa syndrome after L-dopa and selegiline treatment. [electronic resource] by Yosunkaya, Elif Karaca, Ender Basaran, Sarenur Seven, Mehmet Yüksel, Adnan Producer: 20101025 In: Pediatric neurology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Glioma risk associates with polymorphisms of DNA repair genes, XRCC1 and PARP1. [electronic resource] by Yosunkaya, Elif Kucukyuruk, Baris Onaran, Ilhan Gurel, Cigdem B Uzan, Mustafa Kanigur-Sultuybek, Gonul Producer: 20110517 In: British journal of neurosurgery vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication. [electronic resource] by Seven, Mehmet Gezdirici, Alper Ulucan, Hakan Karatas, Omer Faruk Yosunkaya, Elif Yuksel, Adnan Ozen, Mustafa Producer: 20131030 In: Gene vol. 527 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia. [electronic resource] by Gezdirici, Alper Yenigun, Alper Koparir, Erkan Yosunkaya, Elif Ulucan, Hakan Seven, Mehmet Yuksel, Adnan Ozen, Mustafa Producer: 20130517 In: Clinical dysmorphology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Rheumatoid arthritis risk associates with DNA repair gene XRCC1 Arg399Gln polymorphism in Turkish patients. [electronic resource] by Yosunkaya, Elif Karakurt, Funda Cetin, Esra Ozgonenel, Levent Onaran, Ilhan Batar, Bahadir Guven, Mehmet Sultuybek, Gonul Kanigur Producer: 20120821 In: Rheumatology international vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndrome. [electronic resource] by Ulucan, Hakan Koparir, Erkan Koparir, Asuman Karaca, Ender Emre, Ramazan Gezdirici, Alper Yosunkaya, Elif Seven, Mehmet Ozen, Mustafa Yuksel, Adnan Producer: 20130911 In: Clinical dysmorphology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)