Agnese Feresin

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Abdominal Aortic Aneurysm

Top Venues

American journal of medical genetics. Part A

Italian journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Maria Teresa Bonati, Agnese Feresin, Paolo Prontera, Paola Michieletto, Valeria Gambacorta, Giampietro Ricci, Eva Orzan
Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review. Genes 15 (6) (2024)
Maria Teresa Bonati, Agnese Feresin, Paolo Prontera, Paola Michieletto, Valeria Gambacorta, Giampietro Ricci, Eva Orzan
Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review. Genes 15 (6) (2024)
Luciana Musante, Flavio Faletra, Kolja Meier, Hoda Tomoum, Paria Najarzadeh Torbati, Edward Blair, Sally North, Jutta Gärtner, Susann Diegmann, Mehran Beiraghi Toosi, Farah Ashrafzadeh, Ehsan Ghayoor Karimiani, David P Murphy, Flora Maria Murru, Caterina Zanus, Andrea Magnolato, Martina La Bianca, Agnese Feresin, Giorgia Girotto, Paolo Gasparini, Paola Costa, Marco Carrozzi
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition. American journal of medical genetics. Part A 188 (9) (2022)
Francesco Baldo, Laura Morra, Agnese Feresin, Flavio Faletra, Yasmin Al Naber, Luigi Memo, Laura Travan
Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature. Italian journal of pediatrics 48 (1) (2022)
Maria Pina Concas, Massimiliano Cocca, Margherita Francescatto, Thomas Battistuzzi, Beatrice Spedicati, Agnese Feresin, Anna Morgan, Paolo Gasparini, Giorgia Girotto
The Role of Knockout Olfactory Receptor Genes in Odor Discrimination. Genes 12 (5) (2021)