Mariateresa Falco
5PUBLICATIONS
10CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (5)
Sort by Publication Date:
|Nov 27, 2025
Non-Classic Cornelia de Lange Syndrome Due to BRD4 Gene Alterations: A Literature Review.Fortunato Lonardo, Mariateresa Falco, Claudia Costabile
|Sep 27, 2025
MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Prenatal and Postnatal Counseling.Paolo Fontana, Claudia Costabile, Mariateresa Falco
|Apr 03, 2021
Clinical report of a brain magnetic resonance imaging finding in Noonan syndrome.Alessandra D'Amico, Maria Brunella Cipullo, Mariateresa Falco
|Jan 14, 2021
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.Maria Giovanna Tedesco, Fortunato Lonardo, Caterina Ceccarini
|Mar 22, 2017
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings.Mariateresa Falco, Annamaria Franzè, Sandra Iossa
Pageof 1
Frequent Collaborators
3 joint publications
Paolo Fontana
2 joint publications
Fortunato Lonardo
1 joint publications
Chiara Leoni
1 joint publications
Valentina Imperatore
1 joint publications
Paolo Prontera
1 joint publications
Alessandra D'Amico
1 joint publications
Maria Brunella Cipullo
1 joint publications
Lorenzo Ugga
1 joint publications
Daniela Melis
1 joint publications
Maria Rosaria Barillari
