L1CAM variants cause two distinct imaging phenotypes on fetal MRI
- Andrea Accogli
- , Stacy Goergen
- , Giana Izzo
- , Kshitij Mankad
- , Haratz K Krajden
- , Cecilia Parazzini
- , Michael Fahey
- , Lara Menzies
- , Julia Baptista
- , Lucia Carpineta
- , Domenico Tortora
- , Ezio Fulcheri
- , Vellone V Gaetano
- , Dario Paladini
- , Luigina Spaccini
- , Valentina Toto
- , Claire Trayers
- , Sira L Ben
- , Adi Reches
- , Gustavo Malinger
*Corresponding author for this work
- IRCCS Istituto Giannina Gaslini - Genova
- University of Genoa
- Monash Health
- Ospedale dei Bambini Vittore Buzzi
- University College London
- Monash Children’s Hospital Clayton
- Royal Devon & Exeter NHS Foundation Trust
- University of Exeter
- McGill University
- University of Milan
- Cambridge University Hospitals NHS Foundation Trust
- Tel Aviv University
Research output: Contribution to journal › Article › peer-review