A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome. - Arefzadeh, Maryam; Rabbani, Bahareh; Abdolahpour, Saeideh; Emami, Farnoosh; Abbasi, Farzaneh; Masoumi, Tannaz; Mirab Samiee, Siamak; Rabbani, Ali; Mahdieh, Nejat (Clinical Case Reports, 2026)