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Archives of Biochemistry and Biophysics|February 15, 1987
Is the ubiquinone pool in the respiratory chain of the bacterium Paracoccus denitrificans really unhomogeneous?I Kucera, L Kozák, V DadákHuman Genetics|August 2, 2001
Galactosemia: deletion in the 5' upstream region of the GALT gene reduces promoter efficiencyM Trbusek, H Francová, L KozákAmerican Journal of Medical Genetics|May 20, 1999
Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech RepublicV Pekarík, M Blazková, L KozákCasopis Lekaru Ceskych|December 22, 1999
[Direct DNA diagnosis of Friedreich's ataxia]M Borský, V Pekarík, M Tvrdíková, et al.Journal of Inherited Metabolic Disease|January 1, 1993
Haplotype distribution at the phenylalanine hydroxylase locus in PKU families from the Moravian area of CzechoslovakiaL Kozák, D Dvoráková, A Pijácková, et al.Casopis Lekaru Ceskych|May 7, 1997
[Mutation of the phenylalanine hydroxylase gene in the population of central Bohemia. Relation to the clinical picture of phenylketonuria]S Růzicková, L Kozák, M Blazková, et al.Clinical Genetics|March 29, 2008
Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson diseaseL Gojová, E Jansová, M Külm, et al.Casopis Lekaru Ceskych|February 28, 2007
[Genetic databases. Though we were not the first ones, at least let us not to be the last]R Brdicka, R Hradil, L Kozák, et al.Casopis Lekaru Ceskych|June 14, 1995
[Advances in the diagnosis of phenylketonuria with the introduction of direct detection of PAH gene mutation]L Kozák, V Kuhrová, M Blazková, et al.Journal of Medical Genetics|December 10, 1997
Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutationsL Kozák, M Blazková, V Kuhrová, et al.Pageof 2