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M Macek

Showing results (171-180 of 217) with videos related to

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Scientific Reports|November 2, 2023
Entropy in scalp EEG can be used as a preimplantation marker for VNS efficacyB Sklenarova, J Chladek, M Macek, et al.
Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 26, 2025
Novel four-exon deletion in ryanodine receptor gene (RYR2) associated with mixed electric and structural cardiac phenotypeT Stribna, P Peldova, T Vosecka, et al.
Lancet (London, England)|March 29, 1986
First-trimester diagnosis of galactosaemiaW J Kleijer, H C Janse, O P van Diggelen, et al.
Bratislavske Lekarske Listy|July 16, 2004
Separation of Siamese twins in BratislavaJ Siman, J Payer, M Brozman, et al.
Journal of Medical Genetics|August 3, 2004
Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotypeJ Yarden, D Radojkovic, K De Boeck, et al.
Ceskoslovenska Pediatrie|November 1, 1987
[Comparison of the diagnostic effectiveness of prenatal genetic diagnosis in the 1st and 2d trimester of pregnancy]M Macek, H Tomásová, J Hronková, et al.
Human Molecular Genetics|May 16, 1998
A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosisJ E Mickle, M Macek, S B Fulmer-Smentek, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
The experience with the foetal diagnosis of the cystic fibrosis in the second and first trimesterM Macek, H Tomásová, J Boué, et al.
Nature Genetics|June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populationsN Morral, J Bertranpetit, X Estivill, et al.
Pageof 22

Showing results (171-180 of 217) with videos related to

Sort By:
Pageof 22
Scientific Reports|November 2, 2023
Entropy in scalp EEG can be used as a preimplantation marker for VNS efficacyB Sklenarova, J Chladek, M Macek, et al.
Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 26, 2025
Novel four-exon deletion in ryanodine receptor gene (RYR2) associated with mixed electric and structural cardiac phenotypeT Stribna, P Peldova, T Vosecka, et al.
Lancet (London, England)|March 29, 1986
First-trimester diagnosis of galactosaemiaW J Kleijer, H C Janse, O P van Diggelen, et al.
Bratislavske Lekarske Listy|July 16, 2004
Separation of Siamese twins in BratislavaJ Siman, J Payer, M Brozman, et al.
Journal of Medical Genetics|August 3, 2004
Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotypeJ Yarden, D Radojkovic, K De Boeck, et al.
Ceskoslovenska Pediatrie|November 1, 1987
[Comparison of the diagnostic effectiveness of prenatal genetic diagnosis in the 1st and 2d trimester of pregnancy]M Macek, H Tomásová, J Hronková, et al.
Human Molecular Genetics|May 16, 1998
A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosisJ E Mickle, M Macek, S B Fulmer-Smentek, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
The experience with the foetal diagnosis of the cystic fibrosis in the second and first trimesterM Macek, H Tomásová, J Boué, et al.
Nature Genetics|June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populationsN Morral, J Bertranpetit, X Estivill, et al.
Pageof 22