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Cristina Peconi

Showing results (11-20 of 28) with videos related to

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BMC Ophthalmology|April 18, 2014
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucomaEmiliano Giardina, Francesco Oddone, Tiziana Lepre, et al.
Diagnostics (Basel, Switzerland)|January 25, 2025
Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample MonitoringGiulia Trastulli, Giulia Calvino, Bruno Papasergi, et al.
Genes|February 6, 2021
Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human IdentificationMichele Ragazzo, Giulio Puleri, Valeria Errichiello, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 14, 2009
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian populationFederico Ricci, Stefania Zampatti, Francesca D'Abbruzzi, et al.
Human Heredity|May 31, 2006
PSORS2 markers are not associated with psoriatic arthritis in the Italian populationEmiliano Giardina, Irene Predazzi, Cecilia Sinibaldi, et al.
Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.
Genes|October 17, 2019
NGS Analysis for Molecular Diagnosis of Retinitis Pigmentosa (RP): Detection of a Novel Variant in <i>PRPH2</i> GeneClaudia Strafella, Valerio Caputo, Giulia Pagliaroli, et al.
Prenatal Diagnosis|October 11, 2018
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysisStefania Zampatti, Julia Mela, Cristina Peconi, et al.
Neurogenetics|March 27, 2019
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS eraStefania Zampatti, Luca Colantoni, Claudia Strafella, et al.
Frontiers in Neurology|July 3, 2019
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case ReportClaudia Strafella, Giulia Campoli, Rosaria Maria Galota, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
BMC Ophthalmology|April 18, 2014
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucomaEmiliano Giardina, Francesco Oddone, Tiziana Lepre, et al.
Diagnostics (Basel, Switzerland)|January 25, 2025
Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample MonitoringGiulia Trastulli, Giulia Calvino, Bruno Papasergi, et al.
Genes|February 6, 2021
Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human IdentificationMichele Ragazzo, Giulio Puleri, Valeria Errichiello, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 14, 2009
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian populationFederico Ricci, Stefania Zampatti, Francesca D'Abbruzzi, et al.
Human Heredity|May 31, 2006
PSORS2 markers are not associated with psoriatic arthritis in the Italian populationEmiliano Giardina, Irene Predazzi, Cecilia Sinibaldi, et al.
Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.
Genes|October 17, 2019
NGS Analysis for Molecular Diagnosis of Retinitis Pigmentosa (RP): Detection of a Novel Variant in <i>PRPH2</i> GeneClaudia Strafella, Valerio Caputo, Giulia Pagliaroli, et al.
Prenatal Diagnosis|October 11, 2018
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysisStefania Zampatti, Julia Mela, Cristina Peconi, et al.
Neurogenetics|March 27, 2019
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS eraStefania Zampatti, Luca Colantoni, Claudia Strafella, et al.
Frontiers in Neurology|July 3, 2019
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case ReportClaudia Strafella, Giulia Campoli, Rosaria Maria Galota, et al.
Pageof 3