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M Macek

Showing results (181-190 of 217) with videos related to

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American Journal of Human Genetics|July 1, 1996
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosisP W Miller, A Hamosh, M Macek, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Beta-mannosidase deficiency: heterogeneous manifestation in the first female patient and her brotherW J Kleijer, P Hu, R Thoomes, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Stable isotope dilution analysis of N-acetylaspartic acid in CSF, blood, urine and amniotic fluid: accurate postnatal diagnosis and the potential for prenatal diagnosis of Canavan diseaseC Jakobs, H J ten Brink, S A Langelaar, et al.
Human Heredity|January 1, 1995
Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patientsS M Cashman, A Patino, A Martinez, et al.
Acta Universitatis Carolinae. Medica. Monographia|January 1, 1977
Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosisJ Hyánek, V Trnka, J Homolka, et al.
Rozhledy V Chirurgii : Mesicnik Ceskoslovenske Chirurgicke Spolecnosti|August 1, 1975
[Orthotopic liver allotransplantation in pigs (obstruction of the bile ducts, liver sepsis and healing of the graft in the longer-surviving animals)]V Korístek, J Cerný, J Filkuka, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1971
Physical fitness of the Czechoslovak 12-and 15-year-old populationV Seliger, V Cermak, P Handzo, et al.
Physiological Research|January 17, 2007
Pregnancy-associated plasma protein A and proform eosinophilic major basic protein in the detection of different types of coronary artery diseaseP Hájek, M Macek, M Hladíková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Hepatoblastoma, Etiology, Case Reports]A Puchmajerová, A Křepelová, J Indráková, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Pageof 22

Showing results (181-190 of 217) with videos related to

Sort By:
Pageof 22
American Journal of Human Genetics|July 1, 1996
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosisP W Miller, A Hamosh, M Macek, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Beta-mannosidase deficiency: heterogeneous manifestation in the first female patient and her brotherW J Kleijer, P Hu, R Thoomes, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Stable isotope dilution analysis of N-acetylaspartic acid in CSF, blood, urine and amniotic fluid: accurate postnatal diagnosis and the potential for prenatal diagnosis of Canavan diseaseC Jakobs, H J ten Brink, S A Langelaar, et al.
Human Heredity|January 1, 1995
Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patientsS M Cashman, A Patino, A Martinez, et al.
Acta Universitatis Carolinae. Medica. Monographia|January 1, 1977
Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosisJ Hyánek, V Trnka, J Homolka, et al.
Rozhledy V Chirurgii : Mesicnik Ceskoslovenske Chirurgicke Spolecnosti|August 1, 1975
[Orthotopic liver allotransplantation in pigs (obstruction of the bile ducts, liver sepsis and healing of the graft in the longer-surviving animals)]V Korístek, J Cerný, J Filkuka, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1971
Physical fitness of the Czechoslovak 12-and 15-year-old populationV Seliger, V Cermak, P Handzo, et al.
Physiological Research|January 17, 2007
Pregnancy-associated plasma protein A and proform eosinophilic major basic protein in the detection of different types of coronary artery diseaseP Hájek, M Macek, M Hladíková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Hepatoblastoma, Etiology, Case Reports]A Puchmajerová, A Křepelová, J Indráková, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Pageof 22