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	41.	Parental factors in prenatal decision making and the impact of prenatal genetic counseling: a study on Turkish families. [electronic resource] by Simsek-Kiper, P O Utine, G E Volkan-Salanci, B Alanay, Y Aktaş, D Alikaşifoğlu, M Boduroğlu, K Tuncbilek, E Producer: 20140603 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	42.	Angiotensin converting enzyme gene polymorphism and the risk and extent of ischemic heart disease among Turkish patients. [electronic resource] by Tokgözoğlu, S L Alikaşifoğlu, M Atalar, E Tunçbilek, E Ovünç, K Aksöyek, S Kabakçi, G Anar, B Unsal, I Kes, S Producer: 19970904 In: Coronary artery disease vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Higher frequency of allele 2 of the interleukin-1 receptor antagonist gene in patients with juvenile idiopathic arthritis. [electronic resource] by Vencovský, J Jarosová, K Růzicková, S Nemcová, D Niederlová, J Ozen, S Alikasifoglu, M Bakkaloglu, A Ollier, W E Mageed, R A Producer: 20011204 In: Arthritis and rheumatism vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	An eight-case 1q21 region series: novel aberrations and clinical variability with new features. [electronic resource] by Ceylan, A C Sahin, I Erdem, H B Kayhan, G Simsek-Kiper, P O Utine, G E Percin, F Boduroglu, K Alikasifoglu, M Producer: 20200824 In: Journal of intellectual disability research : JIDR vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Identification of point mutations and large rearrangements in the BRCA1 gene in 667 Turkish unselected ovarian cancer patients. [electronic resource] by Aktas, D Gultekin, M Kabacam, S Alikasifoglu, M Turan, A T Tulunay, G Kose, M F Ortac, F Yüce, K Tunçbilek, E Ayhan, A Producer: 20100923 In: Gynecologic oncology vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome. [electronic resource] by Utine, G E Akpınar, B Arslan, U Kiper, P Ö Ş Volkan-Salancı, B Alanay, Y Aktaş, D Haliloğlu, G Oğuz, K K Boduroğlu, K Alikaşifoğlu, M Producer: 20150413 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Genetic IGF1R defects: new cases expand the spectrum of clinical features. [electronic resource] by Gonc, E N Ozon, Z A Oguz, S Kabacam, S Taskiran, E Z Kiper, P O S Utine, G E Alikasifoglu, A Kandemir, N Boduroglu, O K Alikasifoglu, M Producer: 20210827 In: Journal of endocrinological investigation vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	A multidisciplinary approach to the management of individuals with fragile X syndrome. [electronic resource] by Alanay, Y Unal, F Turanli, G Alikaşifoğlu, M Alehan, D Akyol, U Belgin, E Sener, C Aktaş, D Boduroğlu, K Utine, E Volkan-Salanci, B Ozusta, S Genç, A Başar, F Sevinç, S Tunçbilek, E Producer: 20070411 In: Journal of intellectual disability research : JIDR vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)