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	1.	Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family. [electronic resource] by Güran, S Tunca, Y Imirzalioğlu, N Producer: 19990928 In: Cancer genetics and cytogenetics vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic anomalies detected in patients with non-obstructive azoospermia and oligozoospermia. [electronic resource] by Samli, H Samli, M M Solak, M Imirzalioglu, N Producer: 20060810 In: Archives of andrology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD). [electronic resource] by Samli, H Samli, M M Yilmaz, E Imirzalioglu, N Producer: 20061211 In: Archives of andrology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The effects of folic acid application on IL-1beta levels of human gingival fibroblasts stimulated by phenytoin and TNFalpha in vitro: a preliminary study. [electronic resource] by Doğan, A Tunca, Y Ozdemir, A Sengül, A Imirzalioğlu, N Producer: 20020521 In: Journal of oral science vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I. [electronic resource] by Karacay, S Saygun, I Tunca, Y Imirzalioglu, N Guvenc, G Producer: 20070910 In: Journal of the Indian Society of Pedodontics and Preventive Dentistry vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Familial secundum type atrial septal defect with normal karyotypes. [electronic resource] by Buyukates, M Turan, S A Altunkaya, S A Imirzalioglu, N Producer: 20070719 In: The Journal of cardiovascular surgery vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	7.	MEFV gene is a probable susceptibility gene for Behçet's disease. [electronic resource] by Imirzalioglu, N Dursun, A Tastan, B Soysal, Y Yakicier, M C Producer: 20050623 In: Scandinavian journal of rheumatology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders. [electronic resource] by Onrat, S T Emmiler, M Sivaci, Y Söylemez, Z Ozgöz, A Imirzalioğlu, N Producer: 20090825 In: Genetics and molecular research : GMR vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech. [electronic resource] by Soysal, Y Vermeesch, J Davani, N A Şensoy, N Hekimler, K İmirzalıoğlu, N Producer: 20120302 In: Genetics and molecular research : GMR vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Variable clinical expression of Holt-Oram syndrome in three generations. [electronic resource] by Oğur, G Gül, D Lenk, M K Imirzalioğlu, N Alpay, F Oğur, E Producer: 19990415 In: The Turkish journal of pediatrics vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	11.	Prenatal diagnosis of autosomal recessive osteopetrosis, infantile type, by X-ray evaluation. [electronic resource] by Oğur, G Oğur, E Celasun, B Baser, I Imïrzalioğlu, N Oztürk, T Alemdaroğlu, A Producer: 19950921 In: Prenatal diagnosis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure. [electronic resource] by Kahraman, S Bahçe, M Samli, H Imirzalioğlu, N Yakisn, K Cengiz, G Dönmez, E Producer: 20001010 In: Human reproduction (Oxford, England) vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	The vitamin D receptor fokI start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism. [electronic resource] by Bolu, S E Orkunoglu Suer, F E Deniz, F Uckaya, G Imirzalioglu, N Kutlu, M Producer: 20060126 In: Journal of endocrinological investigation vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Application of the 'Apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: results of 30 pregnancies. [electronic resource] by Ogur, G Gül, D Ozen, S Imirzalioglu, N Cankus, G Tunca, Y Bahçe, M Güran, S Baser, I Producer: 19980102 In: Prenatal diagnosis vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Relationship between granular cytoplasm of oocytes and pregnancy outcome following intracytoplasmic sperm injection. [electronic resource] by Kahraman, S Yakin, K Dönmez, E Samli, H Bahçe, M Cengiz, G Sertyel, S Samli, M Imirzalioğlu, N Producer: 20001222 In: Human reproduction (Oxford, England) vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Effect of Helicobacter pylori infection and eradication therapy on interleukin-6 levels in patients with Familial Mediterranean Fever. [electronic resource] by Ozel, A M Demirturk, L Aydogdu, A Gultepe, M Yazgan, Y Imirzalioglu, N Gurbuz, A K Narin, Y Producer: 20080926 In: International journal of clinical practice vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)