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	81.	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)
	82.	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)
	83.	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)
	84.	A comparison of the effect of high-dose methylprednisolone with conventional-dose prednisolone in acute lymphoblastic leukemia patients with randomization. [electronic resource] by Yetgin, S Gürgey, A Tuncer, A M Cetin, M Ozbek, N Sayli, T Güler, E Kara, A Olcay, L Duru, F Gümrük, F Atahan, L Tunçbilek, E Producer: 19980813 In: Leukemia research vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up. [electronic resource] by Yetgin, S Tuncer, M A Cetin, M Gümrük, F Yenicesu, I Tunç, B Oner, A F Toksoy, H Koç, A Aslan, D Ozyürek, E Olcay, L Atahan, L Tunçbilek, E Gürgey, A Producer: 20030411 In: Leukemia vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	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)
	87.	Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. [electronic resource] by Tekin, M Oztürkmen Akay, H Fitoz, S Birnbaum, S Cengiz, F B Sennaroğlu, L Incesulu, A Yüksel Konuk, E B Hasanefendioğlu Bayrak, A Sentürk, S Cebeci, I Utine, G E Tunçbilek, E Nance, W E Duman, D Producer: 20080723 In: Clinical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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