Silvia Bernardo
4PUBLICATIONS
14CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (4)
Sort by Publication Date:
|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
|Oct 19, 2019
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum.Parthiv Haldipur, Kimberly A Aldinger, Silvia Bernardo
|Nov 10, 2017
MRI and US in the evaluation of fetal anomalies: The need to work together.S Bernardo, A Giancotti, A Antonelli
Pageof 1
Frequent Collaborators
2 joint publications
Viviana Caputo
1 joint publications
G Rizzo
1 joint publications
Parthiv Haldipur
1 joint publications
Kimberly A Aldinger
1 joint publications
Conrad Winter
1 joint publications
Steven N Lisgo
1 joint publications
Evelina Silvestri
1 joint publications
Fabien Guimiot
1 joint publications
Rosa Russo
1 joint publications
Debora Kidron
