G. Urel-Demir

Recognizable clinical features of 1p36 deletion syndrome: Insights from a single-center cohort

Objective: 1p36 deletion syndrome is one of the most common contiguous gene deletion syndromes and is primarily characterized by a typical facial gestalt, as well as neurological problems and multisystemic involvement. This study presents the clinical findings of 17 patients with 1p36 deletion syndrome followed at a si...