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	1.	Frequencies of TAP1 and TAP2 gene polymorphisms in the Anatolian population. [electronic resource] by Ozbaş-Gerçeker, F Ozgüç, M Producer: 20031112 In: European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Nucleation-controlled aggregation of deoxyhemoglobin S. Participation of hemoglobin A in the aggregation of deoxyhemoglobin S in concentrated phosphate buffer. [electronic resource] by Adachi, K Ozguc, M Asakura, T Producer: 19800530 In: The Journal of biological chemistry vol. 255 Availability: No items available. Save to lists Add to cart (remove)
	3.	Assessment of housekeeping genes for use in normalization of real time PCR in skeletal muscle with chronic degenerative changes. [electronic resource] by Yüzbaşioğlu, A Onbaşilar, I Kocaefe, C Ozgüç, M Producer: 20100423 In: Experimental and molecular pathology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Deletion analysis in Turkish patients with spinal muscular atrophy. [electronic resource] by Erdem, H Pehlivan, S Topaloglu, H Ozgüç, M Producer: 19990607 In: Brain & development vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families. [electronic resource] by Erdem, H Pehlivan, S Topaloğlu, H Togan, I Ozgüç, M Producer: 19980224 In: The Turkish journal of pediatrics vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	6.	mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girl. [electronic resource] by Topaloğlu, H Seyrantepe, V Kandemir, N Akçören, Z Ozgüç, M Producer: 19980916 In: Pediatric neurology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia. [electronic resource] by Gungor, N Tokath, A Coskun, T Ozguc, M Ozalp, I Producer: 19970114 In: European journal of pediatrics vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Mitochondrial DNA studies in Wolfram (DIDMOAD) syndrome. [electronic resource] by Seyrantepe, V Topaloglu, H Simsek, E Ozguc, M Yordam, N Producer: 19960417 In: Lancet (London, England) vol. 347 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers. [electronic resource] by Seyrantepe, V Kale, G Topaloglu, H Alikasifoglu, A Ozgüc, M Producer: 19991019 In: Brain & development vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. Online. [electronic resource] by Seyrantepe, V Ozguc, M Coskun, T Ozalp, I Reichardt, J K Producer: 19990610 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Myogenic program induction in mature fat tissue (with MyoD expression). [electronic resource] by Kocaefe, Y C Israeli, D Ozguc, M Danos, O Garcia, L Producer: 20050920 In: Experimental cell research vol. 308 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients. [electronic resource] by Ozgüç, M Yilmaz, E Erdem, H Coşkun, T Tokatli, A Ozalp, I Producer: 19950130 In: Journal of inherited metabolic disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Loss of heterozygosity in the VNTR region of intron 1 of P53 in two retinoblastoma cases. [electronic resource] by Emre, S Sungur, A Bilgiç, S Büyükpamukçu, M Günalp, I Ozgüç, M Producer: 19961004 In: Pediatric hematology and oncology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Deletion analysis of Duchenne muscular dystrophy. [electronic resource] by Erdem, H Ayter, S Ozgüç, M Topçu, M Topaloğlu, H Renda, Y Producer: 19931203 In: The Turkish journal of pediatrics vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	15.	Sodium chloride deficiency in cystic fibrosis patients. [electronic resource] by Ozçelik, U Göçmen, A Kiper, N Coşkun, T Yilmaz, E Ozgüç, M Producer: 19950306 In: European journal of pediatrics vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients. [electronic resource] by Ozgüç, M Ozalp, I Coşkun, T Yilmaz, E Erdem, H Ayter, S Producer: 19931203 In: The Turkish journal of pediatrics vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	17.	Mutational analysis of Turkish galactosaemia patients. [electronic resource] by Coskun, T Erkul, E Seyrantepe, V Ozgüç, M Tokatli, A Ozalp, I Producer: 19951213 In: Journal of inherited metabolic disease vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Mutation analysis in Turkish phenylketonuria patients. [electronic resource] by Ozgüç, M Ozalp, I Coşkun, T Yilmaz, E Erdem, H Ayter, S Producer: 19930408 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	DNA haplotype analysis for the diagnosis of Wilson disease in siblings. [electronic resource] by Yüce, A Koçak, N Demirtas, M Ozen, H Gürakan, F Ozgüç, M Producer: 20010329 In: Acta paediatrica (Oslo, Norway : 1992) vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients. [electronic resource] by Dinçer, P Topaloğlu, H Ayter, S Ozgüç, M Taşdemir, H A Renda, Y Producer: 19961105 In: Brain & development vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 41 results.