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Diego Vozzi

Showing results (1-10 of 41) with videos related to

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Gene|November 12, 2013
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing lossFlavio Faletra, Giorgia Girotto, Adamo Pio D'Adamo, et al.
BMC Genetics|December 6, 2014
Genetic landscape of populations along the Silk Road: admixture and migration patternsMassimo Mezzavilla, Diego Vozzi, Nicola Pirastu, et al.
Human Heredity|February 28, 2015
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from QatarMassimo Mezzavilla, Diego Vozzi, Ramin Badii, et al.
Neuron|May 29, 2024
Integrative multi-omic analysis reveals conserved cell-projection deficits in human Down syndrome brainsMohit Rastogi, Martina Bartolucci, Marina Nanni, et al.
Molecular Medicine Reports|August 25, 2015
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome resultsAnna Monica Bianco, Flavio Faletra, Diego Vozzi, et al.
Human Heredity|July 26, 2014
Consanguinity and hereditary hearing loss in QatarGiorgia Girotto, Massimo Mezzavilla, Khalid Abdulhadi, et al.
European Biophysics Journal : EBJ|May 21, 2009
Effect of materials for micro-electro-mechanical systems on PCR yieldCristina Potrich, Lorenzo Lunelli, Stefania Forti, et al.
Journal of Pediatric Hematology/Oncology|November 28, 2017
The Challenge of Next Generation Sequencing in a Boy With Severe Mononucleosis and EBV-related LymphomaFederico Verzegnassi, Erica Valencic, Valentina Kiren, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 31, 2023
MYT1L variant inherited by a mosaic father in a case of severe developmental and epileptic encephalopathySilvia Boeri, Marcello Scala, Francesca Madia, et al.
DNA and Cell Biology|June 24, 2006
Microarray and large-scale in silico--based identification of genes functionally related to Haptoglobin and/or HemopexinSharmila Fagoonee, Ferdinando Di Cunto, Diego Vozzi, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Gene|November 12, 2013
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing lossFlavio Faletra, Giorgia Girotto, Adamo Pio D'Adamo, et al.
BMC Genetics|December 6, 2014
Genetic landscape of populations along the Silk Road: admixture and migration patternsMassimo Mezzavilla, Diego Vozzi, Nicola Pirastu, et al.
Human Heredity|February 28, 2015
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from QatarMassimo Mezzavilla, Diego Vozzi, Ramin Badii, et al.
Neuron|May 29, 2024
Integrative multi-omic analysis reveals conserved cell-projection deficits in human Down syndrome brainsMohit Rastogi, Martina Bartolucci, Marina Nanni, et al.
Molecular Medicine Reports|August 25, 2015
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome resultsAnna Monica Bianco, Flavio Faletra, Diego Vozzi, et al.
Human Heredity|July 26, 2014
Consanguinity and hereditary hearing loss in QatarGiorgia Girotto, Massimo Mezzavilla, Khalid Abdulhadi, et al.
European Biophysics Journal : EBJ|May 21, 2009
Effect of materials for micro-electro-mechanical systems on PCR yieldCristina Potrich, Lorenzo Lunelli, Stefania Forti, et al.
Journal of Pediatric Hematology/Oncology|November 28, 2017
The Challenge of Next Generation Sequencing in a Boy With Severe Mononucleosis and EBV-related LymphomaFederico Verzegnassi, Erica Valencic, Valentina Kiren, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 31, 2023
MYT1L variant inherited by a mosaic father in a case of severe developmental and epileptic encephalopathySilvia Boeri, Marcello Scala, Francesca Madia, et al.
DNA and Cell Biology|June 24, 2006
Microarray and large-scale in silico--based identification of genes functionally related to Haptoglobin and/or HemopexinSharmila Fagoonee, Ferdinando Di Cunto, Diego Vozzi, et al.
Pageof 5