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Veronica Nobile

Showing results (11-20 of 15) with videos related to

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Clinical Genetics|December 14, 2020
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterizationElisabetta Tabolacci, Clelia Molinario, Giuseppe Marangi, et al.
Genes|December 24, 2021
Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double DiagnosisElisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, et al.
Genes|July 27, 2022
Mother and Daughter Carrying of the Same Pathogenic Variant in <i>FGFR2</i> with Discordant PhenotypeFilomena Lo Vecchio, Elisabetta Tabolacci, Veronica Nobile, et al.
NAR Molecular Medicine|February 4, 2026
<i>FMR1</i> RNA interaction with DNMT1 blocks DNA methylation at the <i>FMR1 locus</i>Veronica Nobile, Benedetta Niccolini, Cecilia Pucci, et al.
Human Genetics|January 11, 2020
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 geneVeronica Nobile, Federica Palumbo, Stella Lanni, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Clinical Genetics|December 14, 2020
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterizationElisabetta Tabolacci, Clelia Molinario, Giuseppe Marangi, et al.
Genes|December 24, 2021
Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double DiagnosisElisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, et al.
Genes|July 27, 2022
Mother and Daughter Carrying of the Same Pathogenic Variant in <i>FGFR2</i> with Discordant PhenotypeFilomena Lo Vecchio, Elisabetta Tabolacci, Veronica Nobile, et al.
NAR Molecular Medicine|February 4, 2026
<i>FMR1</i> RNA interaction with DNMT1 blocks DNA methylation at the <i>FMR1 locus</i>Veronica Nobile, Benedetta Niccolini, Cecilia Pucci, et al.
Human Genetics|January 11, 2020
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 geneVeronica Nobile, Federica Palumbo, Stella Lanni, et al.
Pageof 2