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F Prieto

Showing results (151-160 of 157) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish populationE Monrós, J Cañizares, M D Moltó, et al.
Human Genetics|June 1, 1997
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsiesS Bort, E Nelis, V Timmerman, et al.
Circulation|March 1, 1995
Genetic heterogeneity of heart-hand syndromesC T Basson, S D Solomon, B Weissman, et al.
Scientific Reports|October 5, 2018
Modeling the two- and three-dimensional displacement field in Lorca, Spain, subsidence and the global implicationsJose Fernandez, Juan F Prieto, Joaquin Escayo, et al.
Journal of Structural Biology|April 23, 2016
Local analysis of strains and rotations for macromolecular electron microscopy mapsC O S Sorzano, A Martín-Ramos, F Prieto, et al.
British Journal of Haematology|February 26, 2000
Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes. Grupo Cooperativo Español de Citogenética HematológicaF Solé, B Espinet, G F Sanz, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 31, 2025
Laparoscopic surgical resolution of symptomatic biliary pathology during pregnancy: An early therapeutic approach at any gestational ageNicolás Fernandez-Barra, Camila A Fernández, Enzo A Muñoz, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
European Journal of Human Genetics : EJHG|January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish populationE Monrós, J Cañizares, M D Moltó, et al.
Human Genetics|June 1, 1997
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsiesS Bort, E Nelis, V Timmerman, et al.
Circulation|March 1, 1995
Genetic heterogeneity of heart-hand syndromesC T Basson, S D Solomon, B Weissman, et al.
Scientific Reports|October 5, 2018
Modeling the two- and three-dimensional displacement field in Lorca, Spain, subsidence and the global implicationsJose Fernandez, Juan F Prieto, Joaquin Escayo, et al.
Journal of Structural Biology|April 23, 2016
Local analysis of strains and rotations for macromolecular electron microscopy mapsC O S Sorzano, A Martín-Ramos, F Prieto, et al.
British Journal of Haematology|February 26, 2000
Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes. Grupo Cooperativo Español de Citogenética HematológicaF Solé, B Espinet, G F Sanz, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 31, 2025
Laparoscopic surgical resolution of symptomatic biliary pathology during pregnancy: An early therapeutic approach at any gestational ageNicolás Fernandez-Barra, Camila A Fernández, Enzo A Muñoz, et al.
Pageof 16