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B Cabalska

Showing results (11-20 of 20) with videos related to

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Medycyna Wieku Rozwojowego|July 27, 2000
[Evaluation of the usefulness for neonatal mass screening in light of 35 years personal experience]K Bozkowa, B Cabalska, B Radomyska, et al.
Biomedica Biochimica Acta|January 1, 1987
Red blood cell glutathione peroxidase activity as a function of selenium supplementation in dietary treated children with phenylketonuriaB A Zachara, W Wasowicz, J Gromadzińska, et al.
Genetic Testing|September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemiaC Zekanowski, M Nowacka, M Gizewska, et al.
Medycyna Wieku Rozwojowego|October 3, 2000
[Serum tyrosine in children with phenylketonuria and mild hyperphenylalaninemia]B Cabalska, M Nowacka, T Laskowska-Klita, et al.
Molecular and Cellular Probes|August 1, 1994
Frequencies of the most common mutations responsible for phenylketonuria in PolandC Zekanowski, M Nowacka, M Zgulska, et al.
Acta Anthropogenetica|January 1, 1983
Early detection of inborn errors of metabolism in PolandK Bozkowa, B Cabalska, N Duczynska, et al.
Human Genetics|August 31, 1978
PKU locus: genetic linkage with human amylase (Amy) loci and assignment to linkage group IJ Kamarýt, A Mrskos, O Podhradská, et al.
Journal of Intellectual Disability Research : JIDR|January 25, 2003
Different presentations of late-detected phenylketonuria in two brothers with the same R408W/R111X genotype in the PAH geneM Gizewska, B Cabalska, L Cyrytowski, et al.
Medycyna Wieku Rozwojowego|July 27, 2000
[Mutations causing hereditary hyperphenylalaninemia]C Zekanowski, M Nowacka, B Cabalska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1981
[Progress in the early detection of inborn errors of metabolism]K Bozkowa, B Cabalska, N Duczyńska, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Medycyna Wieku Rozwojowego|July 27, 2000
[Evaluation of the usefulness for neonatal mass screening in light of 35 years personal experience]K Bozkowa, B Cabalska, B Radomyska, et al.
Biomedica Biochimica Acta|January 1, 1987
Red blood cell glutathione peroxidase activity as a function of selenium supplementation in dietary treated children with phenylketonuriaB A Zachara, W Wasowicz, J Gromadzińska, et al.
Genetic Testing|September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemiaC Zekanowski, M Nowacka, M Gizewska, et al.
Medycyna Wieku Rozwojowego|October 3, 2000
[Serum tyrosine in children with phenylketonuria and mild hyperphenylalaninemia]B Cabalska, M Nowacka, T Laskowska-Klita, et al.
Molecular and Cellular Probes|August 1, 1994
Frequencies of the most common mutations responsible for phenylketonuria in PolandC Zekanowski, M Nowacka, M Zgulska, et al.
Acta Anthropogenetica|January 1, 1983
Early detection of inborn errors of metabolism in PolandK Bozkowa, B Cabalska, N Duczynska, et al.
Human Genetics|August 31, 1978
PKU locus: genetic linkage with human amylase (Amy) loci and assignment to linkage group IJ Kamarýt, A Mrskos, O Podhradská, et al.
Journal of Intellectual Disability Research : JIDR|January 25, 2003
Different presentations of late-detected phenylketonuria in two brothers with the same R408W/R111X genotype in the PAH geneM Gizewska, B Cabalska, L Cyrytowski, et al.
Medycyna Wieku Rozwojowego|July 27, 2000
[Mutations causing hereditary hyperphenylalaninemia]C Zekanowski, M Nowacka, B Cabalska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1981
[Progress in the early detection of inborn errors of metabolism]K Bozkowa, B Cabalska, N Duczyńska, et al.
Pageof 2