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P Gasparini

Showing results (111-120 of 204) with videos related to

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Human Mutation|November 26, 1999
Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndromeN López-Bigas, R Rabionet, R de Cid, et al.
Annales De Genetique|January 1, 1992
Cystic fibrosis gene mutations and linked RFLPs in the Slovenian populationM Ravnik-Glavac, P Gasparini, B Peterlin, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Clinical Genetics|January 1, 1997
Two mosaic-YY males carrying asymmetric Y chromosomesL Zelante, B Dallapiccola, S Calvano, et al.
The New England Journal of Medicine|September 2, 1999
Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis geneA Pietrangelo, G Montosi, A Totaro, et al.
Human Genetics|September 12, 2000
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) geneR Rabionet, L Zelante, N López-Bigas, et al.
British Journal of Haematology|December 21, 2000
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic backgroundS Perrotta, M D Cappellini, F Bertoldo, et al.
Journal of Medical Genetics|January 1, 1990
The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosisP Gasparini, G Novelli, X Estivill, et al.
Human Genetics|April 1, 1990
Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency. An Italian collaborative studyM Ferrari, M Antonelli, F Bellini, et al.
Human Molecular Genetics|May 1, 1993
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-FP Gasparini, L Borgato, A Piperno, et al.
Pageof 21

Showing results (111-120 of 204) with videos related to

Sort By:
Pageof 21
Human Mutation|November 26, 1999
Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndromeN López-Bigas, R Rabionet, R de Cid, et al.
Annales De Genetique|January 1, 1992
Cystic fibrosis gene mutations and linked RFLPs in the Slovenian populationM Ravnik-Glavac, P Gasparini, B Peterlin, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Clinical Genetics|January 1, 1997
Two mosaic-YY males carrying asymmetric Y chromosomesL Zelante, B Dallapiccola, S Calvano, et al.
The New England Journal of Medicine|September 2, 1999
Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis geneA Pietrangelo, G Montosi, A Totaro, et al.
Human Genetics|September 12, 2000
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) geneR Rabionet, L Zelante, N López-Bigas, et al.
British Journal of Haematology|December 21, 2000
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic backgroundS Perrotta, M D Cappellini, F Bertoldo, et al.
Journal of Medical Genetics|January 1, 1990
The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosisP Gasparini, G Novelli, X Estivill, et al.
Human Genetics|April 1, 1990
Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency. An Italian collaborative studyM Ferrari, M Antonelli, F Bellini, et al.
Human Molecular Genetics|May 1, 1993
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-FP Gasparini, L Borgato, A Piperno, et al.
Pageof 21