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	1.	Laryngomalacia, choanal atresia and renal anomaly in a newborn with Freeman-Sheldon syndrome phenotype. [electronic resource] by Tastekin, A Ikbal, M Ors, R Producer: 20050111 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	2.	Protective role of vitamins A, C, and E against the genotoxic damage induced by aflatoxin B1 in cultured human lymphocytes. [electronic resource] by Alpsoy, L Agar, G Ikbal, M Producer: 20090728 In: Toxicology and industrial health vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Response to Devriendt et al. "Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality". [electronic resource] by Tan, H Ikbal, M Ceviz, N Producer: 20050509 In: American journal of medical genetics. Part A vol. 134A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Micropenis in a newborn with acrocallosal syndrome. [electronic resource] by Ikbal, M Tastekin, A Ors, R Producer: 20041014 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	5.	Association of sister chromatid exchange frequencies in patients with ankylosing spondylitis with and without HLA-B27. [electronic resource] by Ikbal, M Ezirmik, N Tos, T Pirim, I Producer: 20030814 In: Annals of the rheumatic diseases vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Pectus excavatum and situs inversus totalis: a new combination or a coincidence? [electronic resource] by Eroğlu, A Kürkçüoğlu, I C Karaoğlanoğlu, N Ikbal, M Producer: 20041014 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	7.	Linear atrophoderma of Moulin together with leuconychia: a case report. [electronic resource] by Atasoy, M Aliagaoglu, C Sahin, O Ikbal, M Gursan, N Producer: 20060724 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Response to nimodipine in caffeine-induced neurotoxicity in cerebellar granular cell culture of rat pups. [electronic resource] by Gepdiremen, A Sönmez, S Ikbal, M Düzenli, S Tuna, S Producer: 19981120 In: Pharmacological research vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	High frequency of sister chromatid exchanges in lymphocytes of the patients with Behçet's disease. [electronic resource] by Sönmez, S Kaya, M Aktaş, A Ikbal, M Senel, K Producer: 19980422 In: Mutation research vol. 397 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Sister chromatid exchange analysis in patients exposed to low dose of iodine-131 for thyroid scintigraphy. [electronic resource] by Sönmez, S Ikbal, M Yíldírím, M Gepdiremen, A Oztaş, S Producer: 19971223 In: Mutation research vol. 393 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	HLA class I and class II genotyping in patients with Behcet's disease: a regional study of eastern part of Turkey. [electronic resource] by Pirim, I Atasoy, M Ikbal, M Erdem, T Aliagaoglu, C Producer: 20050307 In: Tissue antigens vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A 45 X male patient with 7q distal deletion and rearrangement with SRY gene translocation: a case report. [electronic resource] by Bilen, S Okten, A Karaguzel, G Ikbal, M Aslan, Y Producer: 20140117 In: Genetic counseling (Geneva, Switzerland) vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	13.	Effects of norepinephrine on NMDA-induced neurotoxicity in cerebellar granular cell culture of rat pups. [electronic resource] by Gepdiremen, A Sönmez, S Kiziltunç, A Ikbal, M Erman, F Düzenli, S Producer: 19981222 In: Fundamental & clinical pharmacology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A case of de novo mosaic 18q21.3 deletion with a mild phenotype. [electronic resource] by Alp, M Y Cebi, A H Seyhan, S Cansu, A Ikbal, M Producer: 20140603 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	15.	A case of lower mesodermal defects sequence. [electronic resource] by Tos, T Aktas, S Ikbal, M Avci, M Senel, S Ceylaner, S Producer: 20110302 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	16.	The alteration of sister chromatid exchange frequencies in Behçet's disease with and without HLA-B51. [electronic resource] by Ikbal, M Atasoy, M Pirim, I Aliagaoglu, C Karatay, S Erdem, T Producer: 20060508 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Determination of acute and chronic effects of cadmium on the cardiovascular system of rats. [electronic resource] by Ozturk, Ikbal M Buyukakilli, Belgin Balli, Ebru Cimen, Burak Gunes, Sevgi Erdogan, Semra Producer: 20091117 In: Toxicology mechanisms and methods vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A case of onycotricodysplasia with intellectual disability, without neutropenia. [electronic resource] by Ikbal, M Eker, H K Tos, T Alp, M Y Cebi, A H Producer: 20121120 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	19.	Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report. [electronic resource] by Tos, T Alp, M Y Eker, H K Cebi, A H Ikbal, M Producer: 20140603 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	20.	A Turkish case of subcortical/subependymal heterotopia associated with corpus callosum dysgenesis, craniofacial dysmorphism, severe eye abnormalities, and growth-mental retardation. [electronic resource] by Caksen, H Tuncer, O Ataş, B Demirok, A Unal, O Ikbal, M Odabaş, D Producer: 20040224 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 26 results.