A new 1p36.13-1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis.

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Source: Clinical Genetics - March 12, 2020 Category: Genetics & Stem Cells Authors: Nolting L, Brasch-Andersen C, Cox H, Kanani F, Parker M, Fry AE, Loddo S, Novelli A, Dentici ML, Shelagh J, Jørgensen JP, Fagerberg CR Tags: Clin Genet Source Type: research