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L Bisceglia

Showing results (11-20 of 79) with videos related to

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Human Genetics|April 9, 2005
Gene symbol: SLC3A1. Disease: cystinuriaV Nunes, M font-Llitjós, M Jiménez-Vidal, et al.
Human Genetics|April 9, 2005
Gene symbol: SLC3A1. Disease: cystinuriaV Nunes, M Font-Llitjós, M Jiménez-Vidal, et al.
Human Mutation|March 29, 2000
Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCRJ Purroy, L Bisceglia, J Jaeken, et al.
Human Genetics|April 9, 2005
Gene symbol: SLC3A1. Disease: cystinuriaV Nunes, M Font-Llitjós, M Jiménez-Vidal, et al.
Molecular and Cellular Probes|April 1, 1995
Homozygosity for a novel splice site mutation (2790-2 A--->G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descentC Marigo, C Bombieri, L Bisceglia, et al.
Digestive Diseases and Sciences|April 29, 1998
Polymorphism of motilin gene in patients with Crohn's diseaseV Annese, A Piepoli, A Andriulli, et al.
Molecular and Cellular Probes|June 1, 1995
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria modelS Giannattasio, L Bisceglia, P Lattanzio, et al.
Human Genetics|December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndromeP Gasparini, A Grifa, S Savasta, et al.
Blood|September 18, 1997
Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit geneD Girelli, R Corrocher, L Bisceglia, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|February 26, 2004
[Semiautomatic defibrillators at the workplace health service]G de Nichilo, M S Carucci, L Bisceglia, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
Human Genetics|April 9, 2005
Gene symbol: SLC3A1. Disease: cystinuriaV Nunes, M font-Llitjós, M Jiménez-Vidal, et al.
Human Genetics|April 9, 2005
Gene symbol: SLC3A1. Disease: cystinuriaV Nunes, M Font-Llitjós, M Jiménez-Vidal, et al.
Human Mutation|March 29, 2000
Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCRJ Purroy, L Bisceglia, J Jaeken, et al.
Human Genetics|April 9, 2005
Gene symbol: SLC3A1. Disease: cystinuriaV Nunes, M Font-Llitjós, M Jiménez-Vidal, et al.
Molecular and Cellular Probes|April 1, 1995
Homozygosity for a novel splice site mutation (2790-2 A--->G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descentC Marigo, C Bombieri, L Bisceglia, et al.
Digestive Diseases and Sciences|April 29, 1998
Polymorphism of motilin gene in patients with Crohn's diseaseV Annese, A Piepoli, A Andriulli, et al.
Molecular and Cellular Probes|June 1, 1995
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria modelS Giannattasio, L Bisceglia, P Lattanzio, et al.
Human Genetics|December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndromeP Gasparini, A Grifa, S Savasta, et al.
Blood|September 18, 1997
Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit geneD Girelli, R Corrocher, L Bisceglia, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|February 26, 2004
[Semiautomatic defibrillators at the workplace health service]G de Nichilo, M S Carucci, L Bisceglia, et al.
Pageof 8