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V Romano

Showing results (111-120 of 210) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1988
Chromosomal assignments of human type I and type II cytokeratin genes to different chromosomesV Romano, P Bosco, M Rocchi, et al.
Annali Dell'Istituto Superiore Di Sanita|January 1, 1981
[Statistical studies of infant mortality in Naples in relation to the epidemic of acute respiratory diseases in the winter of 1978-1979]D Greco, N De Ruggiero, R D'Ambrosio, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 3, 2015
Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linkingS Rossi, A Orrico, C Santamaria, et al.
Molecular and Cellular Probes|April 4, 2001
A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemiaV Romano, D Lio, F Calì, et al.
Bioelectromagnetics|January 5, 2008
No evidence of major transcriptional changes in the brain of mice exposed to 1800 MHz GSM signalA Paparini, P Rossi, G Gianfranceschi, et al.
Food Microbiology|May 22, 2012
Occurrence of toxigenic Clostridium difficile in edible bivalve molluscsV Pasquale, V Romano, M Rupnik, et al.
Hybridoma|February 1, 1994
Epitope mapping of human ETS1 monoclonal antibodyN K Bhat, V Romano-Spica, P Georgiou, et al.
Haematologica|November 1, 1982
Genetic heterogeneity of beta thalassemia in western SicilyA Pirrone, A Maggio, R Gambino, et al.
Prenatal Diagnosis|October 1, 1994
Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuriaV Romano, I Dianzani, A Ponzone, et al.
European Journal of Pediatrics|February 9, 1999
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L)G Corsello, P Bosco, F Calì, et al.
Pageof 21

Showing results (111-120 of 210) with videos related to

Sort By:
Pageof 21
Cytogenetics and Cell Genetics|January 1, 1988
Chromosomal assignments of human type I and type II cytokeratin genes to different chromosomesV Romano, P Bosco, M Rocchi, et al.
Annali Dell'Istituto Superiore Di Sanita|January 1, 1981
[Statistical studies of infant mortality in Naples in relation to the epidemic of acute respiratory diseases in the winter of 1978-1979]D Greco, N De Ruggiero, R D'Ambrosio, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 3, 2015
Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linkingS Rossi, A Orrico, C Santamaria, et al.
Molecular and Cellular Probes|April 4, 2001
A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemiaV Romano, D Lio, F Calì, et al.
Bioelectromagnetics|January 5, 2008
No evidence of major transcriptional changes in the brain of mice exposed to 1800 MHz GSM signalA Paparini, P Rossi, G Gianfranceschi, et al.
Food Microbiology|May 22, 2012
Occurrence of toxigenic Clostridium difficile in edible bivalve molluscsV Pasquale, V Romano, M Rupnik, et al.
Hybridoma|February 1, 1994
Epitope mapping of human ETS1 monoclonal antibodyN K Bhat, V Romano-Spica, P Georgiou, et al.
Haematologica|November 1, 1982
Genetic heterogeneity of beta thalassemia in western SicilyA Pirrone, A Maggio, R Gambino, et al.
Prenatal Diagnosis|October 1, 1994
Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuriaV Romano, I Dianzani, A Ponzone, et al.
European Journal of Pediatrics|February 9, 1999
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L)G Corsello, P Bosco, F Calì, et al.
Pageof 21