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Medycyna Wieku Rozwojowego|May 11, 2002
[Biomedical science in the era of complete sequence of human genome]M Jurkowska, J BalActa Biochimica Polonica|January 1, 1992
The frequency of mutations in exon 11 of the CF gene in Polish cystic fibrosis patientsJ Bal, T Mazurczak, J ReissPediatria Polska|March 1, 1996
[Inter-generational transmission of mutations responsible for fragile X syndrome]M Milewski, J Bal, T MazurczakHuman Heredity|November 30, 2000
Association between minihaplotypes and mutations at the PAH locus in Polish hyperphenylalaninemic patientsC Zekanowski, M Jurkowska, J BalPediatria Polska|August 1, 1995
[The type and frequency of mutations in CFTR gene occurrence in patients with cystic fibrosis in Poland--implication of results obtained from genetic counseling and diagnostic screening]J Bal, D Maciejko, T MazurczakActa Microbiologica Polonica|January 1, 1982
Construction of plasmid vectors for gene cloning in Escherichia coli and Bacillus subtilisJ Bal, P Cegłowski, I E MaciagMolecular and Cellular Probes|February 1, 1992
Simple non-radioactive detection of the CFTR mutation N1303K by artificial creation of a restriction siteJ Bal, F Rininsland, L Osborne, et al.Wiadomosci Lekarskie (Warsaw, Poland : 1960)|March 15, 2001
[Identification of mutation and polymorphic changes in the CFTR gene of patients with obstructive azoospermia]A Sobczyńska-Tomaszewska, J K Wolski, J BalPediatria Polska|February 1, 1989
[Study of DNA restriction fragment length polymorphism in the diagnosis of mucoviscidosis]D Maciejko, J Bal, T Mazurczak, et al.Journal of Medical Genetics|January 16, 1998
Molecular basis of mild hyperphenylalaninaemia in PolandC Zekanowski, M Nowacka, B Cabalska, et al.Pageof 5