Francisco Cammarata-Scalisi
8PUBLICATIONS
9CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (8)
Sort by Publication Date:
|Jul 12, 2024
Erratum: Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby
|Jan 01, 2024
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby
|May 16, 2023
Challenges in Communicating a Genetic Diagnosis.Francisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano
|Sep 23, 2022
Extended Overview of Ocular Phenotype with Recent Advances in Hypohidrotic Ectodermal Dysplasia.Michele Callea, Stefano Bignotti, Francesco Semeraro
|Aug 29, 2020
Membranous aplasia cutis congenita in trisomy 18.Francisco Cammarata-Scalisi, Andrea Diociaiuti, Blanca de Guerrero
|Jun 14, 2020
COVID-19 and Down syndrome.Michele Callea, Francisco Cammarata-Scalisi, Angela Galeotti
Pageof 2
Frequent Collaborators
2 joint publications
Colin Eric Willoughby
1 joint publications
Michele Callea
1 joint publications
Angela Galeotti
1 joint publications
Alberto Villani
1 joint publications
Diletta Valentini
1 joint publications
Francesco Semeraro
1 joint publications
Jinia El-Feghaly
1 joint publications
Antonino Morabito
1 joint publications
Vito Romano
