Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA Novel Missense Mutation in the TGF-ß-binding Protein-Like Domain 3 of FBN1 Causes Weill-Marchesani Syndrome with Intellectual Disability.AuthorsHassani, Mahdieh; Taghizadeh, Sara; Broujeni, Anahita Farahzad; Habibi, Mahvash; Banitalebi, Setareh; Kasiri, Mahbubeh; Sadeghi, Alireza; Nozari, AhouraPublicationAdvanced Biomedical Research, 2023, Vol 12, Issue 4, p1ISSN2277-9175Publication typeArticleDOI10.4103/abr.abr_138_22