4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental Delay

Figure 1

Array-based comparative genomic hybridization analysis revealed 2.5 Mb deletion on chromosome 4q25, arr[GRCh38] 4q25(110,513,405_113,009,250)x1 encompassing ENPEP, PANCR, PITX2, MIR297, FAM241A, AP1AR, TIFA, ALPK1, NEUROG2, LOC105377372, ZGRF1, LARP7, MIR302CHG, MIR367, MIR302D, MIR302A, MIR302C, MIR302B, and ANK2.