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	1.	Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic. [electronic resource] by Pekarík, V Blazková, M Kozák, L 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)
	2.	Transition from laminar to turbulent drag in flow due to a vibrating quartz fork. [electronic resource] by Blazková, M Schmoranzer, D Skrbek, L Producer: 20070420 In: Physical review. E, Statistical, nonlinear, and soft matter physics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Hygienic aspects of production of silicon carbide]. [electronic resource] by BERKA, I BLAZKOVA, M KAMENIKOVA, J KLHUFKOVA, E Producer: 20000701 In: Pracovni lekarstvi vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	4.	Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles. [electronic resource] by Popescu, T Blazkova, M Kozak, L Jebeleanu, G Popescu, A Producer: 19981208 In: Human mutation vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	R252W/E178G phenylalanine hydroxylase genotype in a Romanian non-PKU hyperphenylalaninaemic patient. [electronic resource] by Popescu, T Popescu, A Kozak, L Blazkova, M Jebeleanu, G Producer: 19990114 In: Acta paediatrica (Oslo, Norway : 1992) vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Mutation of the phenylalanine hydroxylase gene in the population of central Bohemia. Relation to the clinical picture of phenylketonuria]. [electronic resource] by Růzicková, S Kozák, L Blazková, M Kapras, J St'astná, S Producer: 19970821 In: Casopis lekaru ceskych vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	7.	Ultrafast detection of microsatellite repeat polymorphism in endothelin 1 gene by electrophoresis in short capillaries. [electronic resource] by Klepárnik, K Malá, Z Pribyla, L Blazková, M Vasků, A Bocek, P Producer: 20000211 In: Electrophoresis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations. [electronic resource] by Kozák, L Blazková, M Kuhrová, V Pijácková, A Růzicková, S St'astná, S Producer: 19980130 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Retrospective neuropsychological evaluation of 18 Romanian subjects with hyperphenylalaninaemia. [electronic resource] by Popescu, T Popescu, A Oltean, L Kozak, L Blazkova, M Jebeleanu, G Producer: 20010315 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)
	10.	[Advances in the diagnosis of phenylketonuria with the introduction of direct detection of PAH gene mutation]. [electronic resource] by Kozák, L Kuhrová, V Blazková, M Fajkusová, L Dvoráková, D Pijácková, A Producer: 19951025 In: Casopis lekaru ceskych vol. 134 Availability: No items available. Save to lists Add to cart (remove)
	11.	Fast detection of a (CA)18 microsatellite repeat in the IgE receptor gene by capillary electrophoresis with laser-induced fluorescence detection. [electronic resource] by Klepárník, K Malá, Z Havác, Z Blazková, M Hollá, L Bocek, P Producer: 19980529 In: Electrophoresis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Characterization of two nonsense mutations in the human dystrophin gene. [electronic resource] by Fajkusová, L Pekarík, V Hájek, J Kuhrová, V Blazková, M Fajkus, J Producer: 19990517 In: Journal of neurogenetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families. [electronic resource] by Kozák, L Kuhrová, V Blazková, M Romano, V Fajkusová, L Dvoráková, D Pijácková, A Producer: 19951120 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Polymorphisms in the RAGE gene influence susceptibility to diabetes-associated microvascular dermatoses in NIDDM. [electronic resource] by Kanková, K Záhejský, J Márová, I Muzík, J Kuhrová, V Blazková, M Znojil, V Beránek, M Vácha, J Producer: 20010927 In: Journal of diabetes and its complications vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Angiotensin I-converting enzyme and angiotensinogen gene interaction and prediction of essential hypertension. [electronic resource] by Vasků, A Soucek, M Znojil, V Rihácek, I Tschöplová, S Strelcová, L Cídl, K Blazková, M Hájek, D Hollá, L Vácha, J Producer: 19980803 In: Kidney international vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)