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	21.	[Syndrome of metacentric microchromosome]. [electronic resource] by Zizka, J Balícek, P Lichý, J Marklová, E Maresová, J Producer: 19750905 In: Ceskoslovenska pediatrie vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	22.	A new case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. [electronic resource] by Marklová, E Verner, P Pehal, F Brátová, M Polák, J Producer: 19880412 In: Journal of inherited metabolic disease vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Genetic variants of transferrin in the diagnosis of protein hypoglycosylation. [electronic resource] by Albahri, Z Marklová, E Vanícek, H Minxová, L Dédek, P Skálová, S Producer: 20060705 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	[Pineal tumor with alpha 1 fetoprotein and chorionic gonadotropins in serum and cerebrospinal fluid]. [electronic resource] by Parízek, J Marklová, E Cernoch, Z Nĕmecková, J Dvorák, K Plchová, M Vacuska, M Producer: 19840107 In: Ceskoslovenska neurologie a neurochirurgie vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	25.	Genetic variants of transferrin in cystic fibrosis. [electronic resource] by Marklová, E Albahri, Z Vanícek, H Dedek, P Valis, M Kopácová, M Vávrová, V Producer: 20080909 In: Journal of inherited metabolic disease vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	[Clinical picture of homocystinuria with cystathionine beta-synthase deficiency in 19 Czech and Slovak patients]. [electronic resource] by Orendác, M Kozich, V Zeman, J Hyánek, J Bzdúch, V Misovicová, N Marklová, E Vad'urová, L Pijácková, A Producer: 20010517 In: Casopis lekaru ceskych vol. 139 Availability: No items available. Save to lists Add to cart (remove)
	27.	Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern. [electronic resource] by Mohamed, M Guillard, M Wortmann, S B Cirak, S Marklova, E Michelakakis, H Korsch, E Adamowicz, M Koletzko, B van Spronsen, F J Niezen-Koning, K E Matthijs, G Gardeitchik, T Kouwenberg, D Lim, B Chan Zeevaert, R Wevers, R A Lefeber, D J Morava, E Producer: 20110609 In: Biochimica et biophysica acta vol. 1812 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)