Viviana Caputo
4PUBLICATIONS
8CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (4)
Sort by Publication Date:
|May 31, 2022
Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis.Giulia Napoli, Noemi Panzironi, Alice Traversa
|May 18, 2022
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants.Agnese Giovannetti, Salvatore Daniele Bianco, Alice Traversa
|Jun 11, 2020
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance.Alice Traversa, Enrica Marchionni, Agnese Giovannetti
|Nov 23, 2019
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation.Alice Traversa, Silvia Bernardo, Alessandro Paiardini
Pageof 1
