Ilaria Zito - JoVE Visualize

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American Journal of Medical Genetics. Part A|October 1, 2003

Hereditary nonpolyposis colorectal cancer and related conditionsEmanuela Lucci-Cordisco, Ilaria Zito, Francesca Gensini, et al.

Neuromuscular Disorders : NMD|June 15, 2026

Longitudinal functional trajectories in Duchenne muscular dystrophy: outcome-specific patterns from a registry-based modelling studyAndrea Hörnö-Reissner, Francesca Mattei, Ilaria Zito, et al.

Human Molecular Genetics|November 26, 2004

Molecular dissection of the events leading to inactivation of the FMR1 geneRoberta Pietrobono, Elisabetta Tabolacci, Francesca Zalfa, 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.

Human Mutation|January 29, 2003

Mutations in the CACNA1F and NYX genes in British CSNBX familiesIlaria Zito, Louise E Allen, Reshma J Patel, et al.

Human Molecular Genetics|May 24, 2012

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.

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Showing results (1-10 of 6) with videos related to

Sort By:

Pageof 1

American Journal of Medical Genetics. Part A|October 1, 2003

Hereditary nonpolyposis colorectal cancer and related conditionsEmanuela Lucci-Cordisco, Ilaria Zito, Francesca Gensini, et al.

Neuromuscular Disorders : NMD|June 15, 2026

Longitudinal functional trajectories in Duchenne muscular dystrophy: outcome-specific patterns from a registry-based modelling studyAndrea Hörnö-Reissner, Francesca Mattei, Ilaria Zito, et al.

Human Molecular Genetics|November 26, 2004

Molecular dissection of the events leading to inactivation of the FMR1 geneRoberta Pietrobono, Elisabetta Tabolacci, Francesca Zalfa, 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.

Human Mutation|January 29, 2003

Mutations in the CACNA1F and NYX genes in British CSNBX familiesIlaria Zito, Louise E Allen, Reshma J Patel, et al.

Human Molecular Genetics|May 24, 2012

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.

Pageof 1