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	1.	677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey. [electronic resource] by Boduroglu, K Alikasifoglu, M Anar, B Tuncbilek, E Producer: 19980827 In: Archives of disease in childhood. Fetal and neonatal edition vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects. [electronic resource] by Boduroğlu, K Alikaşifoğlu, M Anar, B Tunçbilek, E Producer: 19990525 In: Journal of child neurology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology. [electronic resource] by Tunçbilek, E Alikasifoğlu, M Boduroğlu, K Aktas, D Anar, B Producer: 19990624 In: American journal of medical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and genetic correlate in childhood onset Friedreich ataxia. [electronic resource] by Alikaşifoglu, M Topaloglu, H Tunçbilek, E Ceviz, N Anar, B Demir, E Ozme, S Producer: 19990818 In: Neuropediatrics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Screening for the fragile X syndrome among mentally retarded males by hair root analysis. [electronic resource] by Tunçbilek, E Alikasifoğlu, M Aktas, D Duman, F Yanik, H Anar, B Oostra, B Willemsen, R Producer: 20010104 In: American journal of medical genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	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)
	7.	Familial aggregation of parkinsonism in progressive supranuclear palsy. [electronic resource] by Donker Kaat, L Boon, A J W Azmani, A Kamphorst, W Breteler, M M B Anar, B Heutink, P van Swieten, J C Producer: 20090807 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations. [electronic resource] by Tamanini, F Bontekoe, C Bakker, C E van Unen, L Anar, B Willemsen, R Yoshida, M Galjaard, H Oostra, B A Hoogeveen, A T Producer: 19990623 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Noninvasive test for fragile X syndrome, using hair root analysis. [electronic resource] by Willemsen, R Anar, B De Diego Otero, Y de Vries, B B Hilhorst-Hofstee, Y Smits, A van Looveren, E Willems, P J Galjaard, H Oostra, B A Producer: 19990805 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Distinct genetic forms of frontotemporal dementia. [electronic resource] by Seelaar, H Kamphorst, W Rosso, S M Azmani, A Masdjedi, R de Koning, I Maat-Kievit, J A Anar, B Donker Kaat, L Breedveld, G J Dooijes, D Rozemuller, J M Bronner, I F Rizzu, P van Swieten, J C Producer: 20081027 In: Neurology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)